메뉴 건너뛰기




Volumn 30, Issue 2, 2013, Pages 307-324

Application of drug nanocrystal technologies on oral drug delivery of poorly soluble drugs

Author keywords

bioavailability; drug nanocrystals; oral drug delivery systems; redispersibility; solidification process

Indexed keywords

5 [1 (3,4 DIMETHOXYBENZOYL) 1,2,3,4 TETRAHYDRO 6 QUINOLYL] 3,6 DIHYDRO 6 METHYL 2H 1,3,4 THIADIAZIN 2 ONE; AMPHOTERICIN B; CILOSTAZOL; CYCLOSPORIN; DANAZOL; FENOFIBRATE; ITRACONAZOLE; MULTIDRUG RESISTANCE PROTEIN; NANOCRYSTAL; NANOPARTICLE;

EID: 84873428567     PISSN: 07248741     EISSN: 1573904X     Source Type: Journal    
DOI: 10.1007/s11095-012-0889-z     Document Type: Review
Times cited : (196)

References (105)
  • 1
    • 0032054501 scopus 로고    scopus 로고
    • Innovative strategies for the oral delivery of drugs and peptides
    • 9586237 1:CAS:528:DyaK1cXisFOjurw%3D
    • Fasano A. Innovative strategies for the oral delivery of drugs and peptides. Trends Biotechnol. 1998;16(4):152-7.
    • (1998) Trends Biotechnol , vol.16 , Issue.4 , pp. 152-157
    • Fasano, A.1
  • 2
    • 60049092472 scopus 로고    scopus 로고
    • Novel platforms for oral drug delivery
    • 19132514 1:CAS:528:DC%2BD1MXktVantQ%3D%3D
    • Colombo P, Sonvico F, Colombo G, Bettini R. Novel platforms for oral drug delivery. Pharm Res. 2009;26(3):601-11.
    • (2009) Pharm Res , vol.26 , Issue.3 , pp. 601-611
    • Colombo, P.1    Sonvico, F.2    Colombo, G.3    Bettini, R.4
  • 3
    • 84862808110 scopus 로고    scopus 로고
    • Fabrication of carvedilol nanosuspensions through the anti-Solvent precipitation-ultrasonication method for the improvement of dissolution rate and oral bioavailability
    • Dandan L, Heming X, Baocheng T, Kun Y, Hao P, Shilin M, et al. Fabrication of carvedilol nanosuspensions through the anti-Solvent precipitation-ultrasonication method for the improvement of dissolution rate and oral bioavailability. AAPS PharmSciTech. 2012;13(1):295-304.
    • (2012) AAPS PharmSciTech , vol.13 , Issue.1 , pp. 295-304
    • Dandan, L.1    Heming, X.2    Baocheng, T.3    Kun, Y.4    Hao, P.5    Shilin, M.6
  • 4
    • 0033805179 scopus 로고    scopus 로고
    • In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs
    • Dressman JB, Reppas C. In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs. Eur J Pharm Sci. 2000;11(S2):73-80.
    • (2000) Eur J Pharm Sci , vol.11 , Issue.S2 , pp. 73-80
    • Dressman, J.B.1    Reppas, C.2
  • 5
    • 77953683770 scopus 로고    scopus 로고
    • Targeting nanoparticles to cancer
    • Wang M, Thanou M. Targeting nanoparticles to cancer. Pharmacol Res. 2010;60(2):90-9.
    • (2010) Pharmacol Res , vol.60 , Issue.2 , pp. 90-99
    • Wang, M.1    Thanou, M.2
  • 6
    • 0036742053 scopus 로고    scopus 로고
    • Poor aqueous solubility - An industry wide problem in drug discovery
    • Lipinski C. Poor aqueous solubility - an industry wide problem in drug discovery. Am Pharm Rev. 2002;5(3):82-5.
    • (2002) Am Pharm Rev , vol.5 , Issue.3 , pp. 82-85
    • Lipinski, C.1
  • 7
    • 75549088273 scopus 로고    scopus 로고
    • Nanoparticles: A personal experience for formulating poorly water soluble drugs
    • 19822177 1:CAS:528:DC%2BC3cXht1Kls7o%3D
    • Cooper ER. Nanoparticles: a personal experience for formulating poorly water soluble drugs. J Control Release. 2010;141(3):300-2.
    • (2010) J Control Release , vol.141 , Issue.3 , pp. 300-302
    • Cooper, E.R.1
  • 8
    • 28444461830 scopus 로고    scopus 로고
    • Drug nanocrystals of poorly soluble drugs produced by high pressure homogenization
    • 16129588 1:CAS:528:DC%2BD2MXht1Ontb7E
    • Keck CM, Müller RH. Drug nanocrystals of poorly soluble drugs produced by high pressure homogenization. Eur J Pharm Biopharm. 2006;62(1):3-16.
    • (2006) Eur J Pharm Biopharm , vol.62 , Issue.1 , pp. 3-16
    • Keck, C.M.1    Müller, R.H.2
  • 9
    • 4544383493 scopus 로고    scopus 로고
    • Nanosuspensions in drug delivery
    • 15340388 1:CAS:528:DC%2BD2cXntFCns7o%3D
    • Rabinow BE. Nanosuspensions in drug delivery. Nat Rev Drug Discov. 2004;3(9):785-96.
    • (2004) Nat Rev Drug Discov , vol.3 , Issue.9 , pp. 785-796
    • Rabinow, B.E.1
  • 10
    • 42549152846 scopus 로고    scopus 로고
    • Drug nanocrystals for the formulation of poorly soluble drugs and its application as a potential drug delivery system
    • 1:CAS:528:DC%2BD1cXkvFajsbg%3D
    • Gao L, Zhang D, Chen M. Drug nanocrystals for the formulation of poorly soluble drugs and its application as a potential drug delivery system. J Nanopart Res. 2008;10(5):845-62.
    • (2008) J Nanopart Res , vol.10 , Issue.5 , pp. 845-862
    • Gao, L.1    Zhang, D.2    Chen, M.3
  • 12
    • 0035937599 scopus 로고    scopus 로고
    • Nanosuspensions as particulate drug formulations in therapy Rationale for development and what we can expect for the future
    • 11251242
    • Müller RH, Jacobs C, Kayser O. Nanosuspensions as particulate drug formulations in therapy Rationale for development and what we can expect for the future. Adv Drug Deliv Rev. 2001;47(1):3-19.
    • (2001) Adv Drug Deliv Rev , vol.47 , Issue.1 , pp. 3-19
    • Müller, R.H.1    Jacobs, C.2    Kayser, O.3
  • 13
    • 34548049483 scopus 로고    scopus 로고
    • Nanosizing - Oral formulation development and biopharmaceutical evaluation
    • 17601629 1:CAS:528:DC%2BD2sXpsFGks7o%3D
    • Kesisoglou F, Panmai S, Wu Y. Nanosizing - oral formulation development and biopharmaceutical evaluation. Adv Drug Deliv Rev. 2007;59(7):631-44.
    • (2007) Adv Drug Deliv Rev , vol.59 , Issue.7 , pp. 631-644
    • Kesisoglou, F.1    Panmai, S.2    Wu, Y.3
  • 14
    • 0024596954 scopus 로고
    • The effect of particle size distribution on dissolution rate and oral absorption
    • 1:CAS:528:DyaL1MXitFyqt7c%3D
    • Hintz RJ, Johnson KC. The effect of particle size distribution on dissolution rate and oral absorption. Int J Pharm. 1989;51(1):9-17.
    • (1989) Int J Pharm , vol.51 , Issue.1 , pp. 9-17
    • Hintz, R.J.1    Johnson, K.C.2
  • 15
    • 0033178415 scopus 로고    scopus 로고
    • Lab-scale production unit design for nanosuspensions of sparingly soluble cytotoxic drugs
    • Böhm BHL, Müller RH. Lab-scale production unit design for nanosuspensions of sparingly soluble cytotoxic drugs. Pharm Sci Tech Today. 1999;2(8):336-9.
    • (1999) Pharm Sci Tech Today , vol.2 , Issue.8 , pp. 336-339
    • Böhm, B.H.L.1    Müller, R.H.2
  • 16
    • 77956882799 scopus 로고    scopus 로고
    • Nanocrystals: Industrially feasible multifunctional formulation technology for poorly soluble actives
    • 20674732 1:CAS:528:DC%2BC3cXhtFOisbzM
    • Shegokar R, Müller RH. Nanocrystals: industrially feasible multifunctional formulation technology for poorly soluble actives. Int J Pharm. 2010;399(1-2):129-39.
    • (2010) Int J Pharm , vol.399 , Issue.1-2 , pp. 129-139
    • Shegokar, R.1    Müller, R.H.2
  • 17
    • 4544275025 scopus 로고    scopus 로고
    • Challenges and solutions for the delivery of biotech drugs - A review of drug nanocrystal technology and lipid nanoparticles
    • 15380654
    • Müller RH, Keck CM. Challenges and solutions for the delivery of biotech drugs - a review of drug nanocrystal technology and lipid nanoparticles. J Biotechnol. 2004;113(1-3):151-70.
    • (2004) J Biotechnol , vol.113 , Issue.1-3 , pp. 151-170
    • Müller, R.H.1    Keck, C.M.2
  • 18
    • 0037312695 scopus 로고    scopus 로고
    • Nanosizing: A formulation approach for poorly-water-soluble compounds
    • 12594003 1:CAS:528:DC%2BD3sXht1Kltrg%3D
    • Merisko-Liversidge E, Liversidge GG, Cooper ER. Nanosizing: a formulation approach for poorly-water-soluble compounds. Eur J Pharm Sci. 2003;18(2):113-20.
    • (2003) Eur J Pharm Sci , vol.18 , Issue.2 , pp. 113-120
    • Merisko-Liversidge, E.1    Liversidge, G.G.2    Cooper, E.R.3
  • 19
    • 1842559836 scopus 로고    scopus 로고
    • Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs
    • 15109023
    • Hu J, Johnston KP, Williams RO. Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs. Drug Dev Ind Pharm. 2004;30(3):233-45.
    • (2004) Drug Dev Ind Pharm , vol.30 , Issue.3 , pp. 233-245
    • Hu, J.1    Johnston, K.P.2    Williams, R.O.3
  • 20
    • 69749103682 scopus 로고    scopus 로고
    • Nanocrystal technology, drug delivery and clinical applications
    • 18990939 1:CAS:528:DC%2BD1cXhtlems7jF
    • Junghanns JAH, Müller RH. Nanocrystal technology, drug delivery and clinical applications. Int J Nanomedicine. 2008;3(3):295-310.
    • (2008) Int J Nanomedicine , vol.3 , Issue.3 , pp. 295-310
    • Junghanns, J.A.H.1    Müller, R.H.2
  • 21
    • 42149190687 scopus 로고    scopus 로고
    • Oral delivery of 1,3-Dicyclohexylurea nanosuspension enhances exposure and lowers blood pressure in hypertensive rats
    • 18312493 1:CAS:528:DC%2BD1cXmtVWgsL0%3D
    • Ghosh S, Chiang P, Wahlstrom JL, Fujiwara H, Selbo JG, Roberds SL. Oral delivery of 1,3-Dicyclohexylurea nanosuspension enhances exposure and lowers blood pressure in hypertensive rats. Basic Clin Pharmacol Toxicol. 2008;102(5):453-8.
    • (2008) Basic Clin Pharmacol Toxicol , vol.102 , Issue.5 , pp. 453-458
    • Ghosh, S.1    Chiang, P.2    Wahlstrom, J.L.3    Fujiwara, H.4    Selbo, J.G.5    Roberds, S.L.6
  • 22
    • 79952922229 scopus 로고    scopus 로고
    • A formulation comparison between micro- and nanosuspensions: The importance of particle size for absorption of a model compound, following repeated oral administration to rats during early development
    • 20653464 1:CAS:528:DC%2BC3MXptFah
    • Sigfridsson K, Nordmark A, Theilig S, Lindah A. A formulation comparison between micro- and nanosuspensions: the importance of particle size for absorption of a model compound, following repeated oral administration to rats during early development. Drug Dev Ind Pharm. 2011;37(2):185-92.
    • (2011) Drug Dev Ind Pharm , vol.37 , Issue.2 , pp. 185-192
    • Sigfridsson, K.1    Nordmark, A.2    Theilig, S.3    Lindah, A.4
  • 23
    • 20844446627 scopus 로고    scopus 로고
    • The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: A beagle dog model predicts improved bioavailability and diminished food effect on absorption in human
    • 15488686 1:CAS:528:DC%2BD2cXosFSrsbg%3D
    • Wu Y, Loper A, Landis E, Hettrick L, Novak L, Lynn K, et al. The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: a beagle dog model predicts improved bioavailability and diminished food effect on absorption in human. Int J Pharm. 2004;285(1-2):135-46.
    • (2004) Int J Pharm , vol.285 , Issue.1-2 , pp. 135-146
    • Wu, Y.1    Loper, A.2    Landis, E.3    Hettrick, L.4    Novak, L.5    Lynn, K.6
  • 24
    • 34547781194 scopus 로고    scopus 로고
    • A formulation comparison, using a solution and different nanosuspensions of a poorly soluble compound
    • 17383167 1:CAS:528:DC%2BD2sXovFyrs74%3D
    • Sigfridsson K, Forssén S, Holländer P, Skantze U, de Verdier J. A formulation comparison, using a solution and different nanosuspensions of a poorly soluble compound. Eur J Pharm Biopharm. 2007;67(2):540-7.
    • (2007) Eur J Pharm Biopharm , vol.67 , Issue.2 , pp. 540-547
    • Sigfridsson, K.1    Forssén, S.2    Holländer, P.3    Skantze, U.4    De Verdier, J.5
  • 25
    • 61349191553 scopus 로고    scopus 로고
    • Enhancement of oral bioavailability of an HIV-attachment inhibitor by nanosizing and amorphous formulation approaches
    • 19100319 1:CAS:528:DC%2BD1MXislKisLc%3D
    • Fakes MG, Vakkalagadda BJ, Qian F, Desikan S, Gandhi RB, Lai C, et al. Enhancement of oral bioavailability of an HIV-attachment inhibitor by nanosizing and amorphous formulation approaches. Int J Pharm. 2009;370(1-2):167-74.
    • (2009) Int J Pharm , vol.370 , Issue.1-2 , pp. 167-174
    • Fakes, M.G.1    Vakkalagadda, B.J.2    Qian, F.3    Desikan, S.4    Gandhi, R.B.5    Lai, C.6
  • 26
    • 33344478634 scopus 로고    scopus 로고
    • Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs
    • 16410029 1:CAS:528:DC%2BD28XhslKjtL0%3D
    • Jinno J, Kamada N, Miyake M, Yamada K, Mukai T, Odomi M, et al. Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs. J Control Release. 2006;111(1-2):56-64.
    • (2006) J Control Release , vol.111 , Issue.1-2 , pp. 56-64
    • Jinno, J.1    Kamada, N.2    Miyake, M.3    Yamada, K.4    Mukai, T.5    Odomi, M.6
  • 27
    • 33744973517 scopus 로고    scopus 로고
    • Oral bioavailability of cyclosporine: Solid lipid nanoparticles (SLN®) versus drug nanocrystals
    • 16580159
    • Müller RH, Runge S, Ravelli V, Mehnert W, Thünemann AF, Souto EB. Oral bioavailability of cyclosporine: Solid lipid nanoparticles (SLN®) versus drug nanocrystals. Int J Pharm. 2006;317(1):82-9.
    • (2006) Int J Pharm , vol.317 , Issue.1 , pp. 82-89
    • Müller, R.H.1    Runge, S.2    Ravelli, V.3    Mehnert, W.4    Thünemann, A.F.5    Souto, E.B.6
  • 28
    • 0029080002 scopus 로고
    • Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs
    • 1:CAS:528:DyaK2MXot12jsr0%3D
    • Liversidge GG, Cundy KC. Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs. Int J Pharm. 1995;125(1):91-7.
    • (1995) Int J Pharm , vol.125 , Issue.1 , pp. 91-97
    • Liversidge, G.G.1    Cundy, K.C.2
  • 29
    • 37849026020 scopus 로고    scopus 로고
    • Cogrinding enhances the oral bioavailability of EMD 57033, a poorly water soluble drug, in dogs
    • 17646091 1:CAS:528:DC%2BD1cXlsF2rtw%3D%3D
    • Vogt M, Vertzoni M, Kunath K, Reppas C, Dressman JB. Cogrinding enhances the oral bioavailability of EMD 57033, a poorly water soluble drug, in dogs. Eur J Pharm Biopharm. 2008;68(2):338-45.
    • (2008) Eur J Pharm Biopharm , vol.68 , Issue.2 , pp. 338-345
    • Vogt, M.1    Vertzoni, M.2    Kunath, K.3    Reppas, C.4    Dressman, J.B.5
  • 30
    • 70350639421 scopus 로고    scopus 로고
    • Preparation of fenofibrate nanosuspension and study of its pharmacokinetic behavior in rats
    • 19466879 1:CAS:528:DC%2BD1MXnt1Sitbw%3D
    • Li X, Gu L, Xu Y, Wang Y. Preparation of fenofibrate nanosuspension and study of its pharmacokinetic behavior in rats. Drug Dev Ind Pharm. 2009;35(7):827-33.
    • (2009) Drug Dev Ind Pharm , vol.35 , Issue.7 , pp. 827-833
    • Li, X.1    Gu, L.2    Xu, Y.3    Wang, Y.4
  • 31
    • 34547863131 scopus 로고    scopus 로고
    • Pharmacokinetic evaluation of oral fenofibrate nanosuspensions and SLN in comparison to conventional suspensions of micronized drug
    • 17566595 1:CAS:528:DC%2BD2sXpt1Cqtr0%3D
    • Hanafy A, Spahn-Langguth H, Vergnault G, Grenier P, Tubic Grozdanis M, Lenhardt T, et al. Pharmacokinetic evaluation of oral fenofibrate nanosuspensions and SLN in comparison to conventional suspensions of micronized drug. Adv Drug Deliv Rev. 2007;59(6):419-26.
    • (2007) Adv Drug Deliv Rev , vol.59 , Issue.6 , pp. 419-426
    • Hanafy, A.1    Spahn-Langguth, H.2    Vergnault, G.3    Grenier, P.4    Tubic Grozdanis, M.5    Lenhardt, T.6
  • 32
    • 79958005215 scopus 로고    scopus 로고
    • Potent dried drug nanosuspensions for oral bioavailability enhancement of poorly soluble drugs with pH-dependent solubility
    • 21540090 1:CAS:528:DC%2BC3MXmvFOiu7s%3D
    • Mou D, Chen H, Wan J, Xu H, Yang X. Potent dried drug nanosuspensions for oral bioavailability enhancement of poorly soluble drugs with pH-dependent solubility. Int J Pharm. 2011;413(1-2):237-44.
    • (2011) Int J Pharm , vol.413 , Issue.1-2 , pp. 237-244
    • Mou, D.1    Chen, H.2    Wan, J.3    Xu, H.4    Yang, X.5
  • 33
    • 0037142222 scopus 로고    scopus 로고
    • In vivo evaluation of matrix pellets containing nanocrystalline ketoprofen
    • 12062503 1:CAS:528:DC%2BD38Xktlaru7w%3D
    • Vergote GJ, Vervaet C, Van Driessche I, Hoste S, De Smedt S, Demeester J, et al. In vivo evaluation of matrix pellets containing nanocrystalline ketoprofen. Int J Pharm. 2002;240(1-2):79-84.
    • (2002) Int J Pharm , vol.240 , Issue.1-2 , pp. 79-84
    • Vergote, G.J.1    Vervaet, C.2    Van Driessche, I.3    Hoste, S.4    De Smedt, S.5    Demeester, J.6
  • 34
    • 0028824401 scopus 로고
    • Drug particle size reduction for decreasing gastric irritancy and enhancing absorption of naproxen in rats
    • 1:CAS:528:DyaK2MXoslGmsbg%3D
    • Liversidge GG, Conzentino P. Drug particle size reduction for decreasing gastric irritancy and enhancing absorption of naproxen in rats. Int J Pharm. 1995;125(2):309-13.
    • (1995) Int J Pharm , vol.125 , Issue.2 , pp. 309-313
    • Liversidge, G.G.1    Conzentino, P.2
  • 35
    • 16244398708 scopus 로고    scopus 로고
    • Nanosuspension formulations for low-soluble drugs: Pharmacokinetic evaluation using spironolactone as model compound
    • 15830727 1:CAS:528:DC%2BD2MXjsVaqtL0%3D
    • Langguth P, Hanafy A, Frenzel D, Grenier P, Nhamias A, Ohlig T, et al. Nanosuspension formulations for low-soluble drugs: pharmacokinetic evaluation using spironolactone as model compound. Drug Dev Ind Pharm. 2005;31(3):319-29.
    • (2005) Drug Dev Ind Pharm , vol.31 , Issue.3 , pp. 319-329
    • Langguth, P.1    Hanafy, A.2    Frenzel, D.3    Grenier, P.4    Nhamias, A.5    Ohlig, T.6
  • 36
    • 71049183092 scopus 로고    scopus 로고
    • Particle size reduction for improvement of oral absorption absorption of the poorly soluble drug UG558 in rats during early development
    • 19929207 1:CAS:528:DC%2BD1MXhsVGlt7vL
    • Sigfridsson K, Lundqvist AJ, Strimfors M. Particle size reduction for improvement of oral absorption absorption of the poorly soluble drug UG558 in rats during early development. Drug Dev Ind Pharm. 2009;35(12):1479-86.
    • (2009) Drug Dev Ind Pharm , vol.35 , Issue.12 , pp. 1479-1486
    • Sigfridsson, K.1    Lundqvist, A.J.2    Strimfors, M.3
  • 37
    • 78650679438 scopus 로고    scopus 로고
    • Preparation of a chemically stable quercetin formulation using nanosuspension technology
    • 21093559 1:CAS:528:DC%2BC3cXhs1SrtL7J
    • Gao L, Liu G, Wang X, Liu F, Xu Y, Ma J. Preparation of a chemically stable quercetin formulation using nanosuspension technology. Int J Pharm. 2011;404(1-2):231-7.
    • (2011) Int J Pharm , vol.404 , Issue.1-2 , pp. 231-237
    • Gao, L.1    Liu, G.2    Wang, X.3    Liu, F.4    Xu, Y.5    Ma, J.6
  • 38
    • 0037189994 scopus 로고    scopus 로고
    • Enhanced drug dissolution using evaporative precipitation into aqueous solution
    • 12176292 1:CAS:528:DC%2BD38Xmt1ygt7c%3D
    • Sarkari M, Brown J, Chen X, Swinnea S, Williams III RO, Johnston KP. Enhanced drug dissolution using evaporative precipitation into aqueous solution. Int J Pharm. 2002;243(1-2):17-31.
    • (2002) Int J Pharm , vol.243 , Issue.1-2 , pp. 17-31
    • Sarkari, M.1    Brown, J.2    Chen, X.3    Swinnea, S.4    Williams Iii, R.O.5    Johnston, K.P.6
  • 39
    • 0031402134 scopus 로고    scopus 로고
    • Mucoadhesion of colloidal particulate systems in the gastro-intestinal tract
    • 1:CAS:528:DyaK2sXmtFShtr0%3D
    • Ponchel G, Montisci MJ, Dembri A, Durrer C, Duchêne D. Mucoadhesion of colloidal particulate systems in the gastro-intestinal tract. Eur J Pharm Biopharm. 1997;44(1):25-31.
    • (1997) Eur J Pharm Biopharm , vol.44 , Issue.1 , pp. 25-31
    • Ponchel, G.1    Montisci, M.J.2    Dembri, A.3    Durrer, C.4    Duchêne, D.5
  • 40
    • 0345267135 scopus 로고    scopus 로고
    • Bioadhesion of solid oral dosage forms, why and how?
    • Duchêne D, Ponchel G. Bioadhesion of solid oral dosage forms, why and how? Eur J Pharm Biopharm. 1997;44(1):15-23.
    • (1997) Eur J Pharm Biopharm , vol.44 , Issue.1 , pp. 15-23
    • Duchêne, D.1    Ponchel, G.2
  • 41
    • 17444372009 scopus 로고    scopus 로고
    • Mucoadhesives in the gastrointestinal tract: Revisiting the literature for novel applications
    • 15848050 1:CAS:528:DC%2BD2MXjsVehsLg%3D
    • Dodou D, Breedveld P, Wieringa PA. Mucoadhesives in the gastrointestinal tract: revisiting the literature for novel applications. Eur J Pharm Biopharm. 2005;60(1):1-16.
    • (2005) Eur J Pharm Biopharm , vol.60 , Issue.1 , pp. 1-16
    • Dodou, D.1    Breedveld, P.2    Wieringa, P.A.3
  • 42
    • 26644454810 scopus 로고    scopus 로고
    • The basics and underlying mechanisms of mucoadhesion
    • 16198441 1:CAS:528:DC%2BD2MXhtFSis7fP
    • Smart JD. The basics and underlying mechanisms of mucoadhesion. Adv Drug Deliv Rev. 2005;57(11):1556-68.
    • (2005) Adv Drug Deliv Rev , vol.57 , Issue.11 , pp. 1556-1568
    • Smart, J.D.1
  • 43
    • 0035910888 scopus 로고    scopus 로고
    • A new approach for targeting to Cryptosporidium parvum using mucoadhesive nanosuspensions: Research and applications
    • 11282242 1:CAS:528:DC%2BD3MXitFWgsLs%3D
    • Kayser O. A new approach for targeting to Cryptosporidium parvum using mucoadhesive nanosuspensions: research and applications. Int J Pharm. 2001;214(1-2):83-5.
    • (2001) Int J Pharm , vol.214 , Issue.1-2 , pp. 83-85
    • Kayser, O.1
  • 44
    • 84862685036 scopus 로고    scopus 로고
    • Imaging of size-dependent uptake and identification of novel pathways in mouse Peyer's patches using fluorescent organosilica particles
    • 21889475 1:CAS:528:DC%2BC38XptVKlu7g%3D
    • Awaad A, Nakamura M, Ishimura K. Imaging of size-dependent uptake and identification of novel pathways in mouse Peyer's patches using fluorescent organosilica particles. Nanomedicine. 2012;8(5):627-36.
    • (2012) Nanomedicine , vol.8 , Issue.5 , pp. 627-636
    • Awaad, A.1    Nakamura, M.2    Ishimura, K.3
  • 45
    • 33748885473 scopus 로고    scopus 로고
    • Low molecular weight heparin nanoparticles: Mucoadhesion and behaviour in Caco-2 cells
    • 1:CAS:528:DC%2BD28XhtVSrsb%2FO
    • Lamprecht A, Koenig P, Ubrich N, Maincent P, Neumann D. Low molecular weight heparin nanoparticles: mucoadhesion and behaviour in Caco-2 cells. Nanotechnology. 2006;17(15):3673-80.
    • (2006) Nanotechnology , vol.17 , Issue.15 , pp. 3673-3680
    • Lamprecht, A.1    Koenig, P.2    Ubrich, N.3    Maincent, P.4    Neumann, D.5
  • 46
    • 0033496577 scopus 로고    scopus 로고
    • Relative bioavailability and effects of a high fat meal on single dose cilostazol pharmacokinetics
    • 10702883 1:CAS:528:DC%2BD3cXhs1Gns70%3D
    • Bramer SL, Forbes WP. Relative bioavailability and effects of a high fat meal on single dose cilostazol pharmacokinetics. Clin Pharmacokinet. 1999;37 Suppl 2:13-23.
    • (1999) Clin Pharmacokinet , vol.37 , Issue.SUPPL. 2 , pp. 13-23
    • Bramer, S.L.1    Forbes, W.P.2
  • 47
    • 32544458008 scopus 로고    scopus 로고
    • Absence of a food effect with a 145 mg nanoparticle fenofibrate tablet formulation
    • 16502765 1:CAS:528:DC%2BD28XhvVSgtr4%3D
    • Sauron R, Wilkins M, Jessent V, Dubois A, Maillot C, Weil A. Absence of a food effect with a 145 mg nanoparticle fenofibrate tablet formulation. Int J Clin Pharmacol Ther. 2006;44(2):64-70.
    • (2006) Int J Clin Pharmacol Ther , vol.44 , Issue.2 , pp. 64-70
    • Sauron, R.1    Wilkins, M.2    Jessent, V.3    Dubois, A.4    Maillot, C.5    Weil, A.6
  • 48
    • 0032402219 scopus 로고    scopus 로고
    • Evaluation of nano- and microparticle uptake by the gastrointestinal tract
    • 10837679 1:CAS:528:DyaK1cXnsFWlt7w%3D
    • Delie F. Evaluation of nano- and microparticle uptake by the gastrointestinal tract. Adv Drug Deliv Rev. 1998;34(2-3):221-33.
    • (1998) Adv Drug Deliv Rev , vol.34 , Issue.2-3 , pp. 221-233
    • Delie, F.1
  • 49
    • 79955978422 scopus 로고    scopus 로고
    • Poly(lactide-co-glycolide) nanoparticles for peroral delivery of bioactives
    • 1:CAS:528:DC%2BC3MXmtlGnt7Y%3D
    • Grama CN, Ankola DD, Ravi Kumar MNV. Poly(lactide-co-glycolide) nanoparticles for peroral delivery of bioactives. Curr Opin Colloid Interface Sci. 2011;16(3):238-45.
    • (2011) Curr Opin Colloid Interface Sci , vol.16 , Issue.3 , pp. 238-245
    • Grama, C.N.1    Ankola, D.D.2    Ravi Kumar, M.N.V.3
  • 50
    • 0030471901 scopus 로고    scopus 로고
    • Gastrointestinal uptake of biodegradable microparticles: Effect of particle size
    • 8987081 1:CAS:528:DyaK2sXltVSquw%3D%3D
    • Desai MP, Labhasetwar V, Amidon GL, Levy RJ. Gastrointestinal uptake of biodegradable microparticles: effect of particle size. Pharm Res. 1996;13(12):1838-45.
    • (1996) Pharm Res , vol.13 , Issue.12 , pp. 1838-1845
    • Desai, M.P.1    Labhasetwar, V.2    Amidon, G.L.3    Levy, R.J.4
  • 51
    • 33751253462 scopus 로고    scopus 로고
    • Nanoparticles as potential oral delivery systems of proteins and vaccines: A mechanistic approach
    • 17050027
    • des Rieux A, Fievez V, Garinot M, Schneider YJ, Préat V. Nanoparticles as potential oral delivery systems of proteins and vaccines: a mechanistic approach. J Control Release. 2006;116(1):1-27.
    • (2006) J Control Release , vol.116 , Issue.1 , pp. 1-27
    • Des Rieux, A.1    Fievez, V.2    Garinot, M.3    Schneider, Y.J.4    Préat, V.5
  • 52
    • 0032714228 scopus 로고    scopus 로고
    • Inhibition of P-glycoprotein by D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS)
    • 10554096 1:CAS:528:DyaK1MXntVOhtbg%3D
    • Dintaman JM, Silverman JA. Inhibition of P-glycoprotein by D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS). Pharm Res. 1999;16(10):1550-6.
    • (1999) Pharm Res , vol.16 , Issue.10 , pp. 1550-1556
    • Dintaman, J.M.1    Silverman, J.A.2
  • 53
    • 84862889539 scopus 로고    scopus 로고
    • Development of a precipitation-resistant solution formulation to increase in vivo exposure of a poorly water-soluble compound
    • 22569200 1:CAS:528:DC%2BC38XotFKmu7s%3D
    • Burton L, Ying W, Gandhi R, West R, Huang C, Zhou S, et al. Development of a precipitation-resistant solution formulation to increase in vivo exposure of a poorly water-soluble compound. Int J Pharm. 2012;433(1-2):94-101.
    • (2012) Int J Pharm , vol.433 , Issue.1-2 , pp. 94-101
    • Burton, L.1    Ying, W.2    Gandhi, R.3    West, R.4    Huang, C.5    Zhou, S.6
  • 54
    • 77953359223 scopus 로고    scopus 로고
    • The effects of excipients on transporter mediated absorption
    • 1:CAS:528:DC%2BC3cXms1elsLk%3D
    • Goole J, Lindley DJ, Roth W, Carl SM, Amighi K, Kauffmann JM, et al. The effects of excipients on transporter mediated absorption. Int Pharm. 2010;393(1-2):17-31.
    • (2010) Int Pharm , vol.393 , Issue.1-2 , pp. 17-31
    • Goole, J.1    Lindley, D.J.2    Roth, W.3    Carl, S.M.4    Amighi, K.5    Kauffmann, J.M.6
  • 55
    • 42649107490 scopus 로고    scopus 로고
    • Effect of pluronic F68 block copolymer on P-glycoprotein transport and CYP3A4 metabolism
    • 18242899 1:CAS:528:DC%2BD1cXlsFCks7Y%3D
    • Huang J, Si L, Jiang L, Fan Z, Qiu J, Li G. Effect of pluronic F68 block copolymer on P-glycoprotein transport and CYP3A4 metabolism. Int J Pharm. 2008;356(1-2):351-3.
    • (2008) Int J Pharm , vol.356 , Issue.1-2 , pp. 351-353
    • Huang, J.1    Si, L.2    Jiang, L.3    Fan, Z.4    Qiu, J.5    Li, G.6
  • 56
    • 61449188212 scopus 로고    scopus 로고
    • Inhibiting efflux with novel non-ionic surfactants: Rational design based on vitamin e TPGS
    • Wempe MF, Wright C, Little JL, Lightner JW, Large SE, Caflisch GB, et al. Inhibiting efflux with novel non-ionic surfactants: Rational design based on vitamin E TPGS. Int J Pharm. 2009;3701-2:93-102.
    • (2009) Int J Pharm , vol.3701 , Issue.2 , pp. 93-102
    • Wempe, M.F.1    Wright, C.2    Little, J.L.3    Lightner, J.W.4    Large, S.E.5    Caflisch, G.B.6
  • 57
    • 0037378033 scopus 로고    scopus 로고
    • Minireview: In vivo pharmacodynamics of antifungal drugs in treatment of candidiasis
    • Andes D. Minireview: in vivo pharmacodynamics of antifungal drugs in treatment of candidiasis. Antimicrob Agents Chemother. 2003;474:1179-786.
    • (2003) Antimicrob Agents Chemother , vol.474 , pp. 1179-1786
    • Andes, D.1
  • 59
    • 0037453179 scopus 로고    scopus 로고
    • Formulation of amphotericin B as nanosuspension for oral administration
    • Kayser O, Olbrich C, Yardley V, Kiderlen AF, Croft SL. Formulation of amphotericin B as nanosuspension for oral administration. Int J Pharm. 2003;2541:73-5.
    • (2003) Int J Pharm , vol.2541 , pp. 73-75
    • Kayser, O.1    Olbrich, C.2    Yardley, V.3    Kiderlen, A.F.4    Croft, S.L.5
  • 60
    • 33645030096 scopus 로고    scopus 로고
    • Preparation and evaluation of nanosuspensions for enhancing the dissolution of poorly soluble drugs
    • Kocbek P, Baumgartner S, Kristl J. Preparation and evaluation of nanosuspensions for enhancing the dissolution of poorly soluble drugs. Int J Pharm. 2006;3121-2:179-86.
    • (2006) Int J Pharm , vol.3121 , Issue.2 , pp. 179-186
    • Kocbek, P.1    Baumgartner, S.2    Kristl, J.3
  • 61
    • 33646515151 scopus 로고    scopus 로고
    • A phase i study with oral SU5416 in patients with advanced solid tumors: A drug inducing its clearance
    • Salzberg M, Pless M, Rochlitz C, Ambrus K, Scigalla P, Herrmann R. A phase I study with oral SU5416 in patients with advanced solid tumors: a drug inducing its clearance. Invest New Drugs. 2006;244:299-304.
    • (2006) Invest New Drugs , vol.244 , pp. 299-304
    • Salzberg, M.1    Pless, M.2    Rochlitz, C.3    Ambrus, K.4    Scigalla, P.5    Herrmann, R.6
  • 62
    • 84864126060 scopus 로고    scopus 로고
    • Enhanced solubility and oral bioavailability of itraconazole by combining membrane emulsification and spray drying technique
    • Choi YK, Poudel BK, Marasini N, Yang KY, Kim JW, Kim JO, et al. Enhanced solubility and oral bioavailability of itraconazole by combining membrane emulsification and spray drying technique. Int J Pharm. 2012;4341-2:264-71.
    • (2012) Int J Pharm , vol.4341 , Issue.2 , pp. 264-271
    • Choi, Y.K.1    Poudel, B.K.2    Marasini, N.3    Yang, K.Y.4    Kim, J.W.5    Kim, J.O.6
  • 63
    • 53049095815 scopus 로고    scopus 로고
    • Microcrystalline cellulose, a useful alternative for sucrose as a matrix former during freeze-drying of drug nanosuspensions - A case study with itraconazole
    • Van Eerdenbrugh B, Vercruysse S, Martens JA, Vermant J, Froyen L, Van Humbeeck J, et al. Microcrystalline cellulose, a useful alternative for sucrose as a matrix former during freeze-drying of drug nanosuspensions - a case study with itraconazole. Eur J Pharm Biopharm. 2008;702:590-6.
    • (2008) Eur J Pharm Biopharm , vol.702 , pp. 590-596
    • Van Eerdenbrugh, B.1    Vercruysse, S.2    Martens, J.A.3    Vermant, J.4    Froyen, L.5    Van Humbeeck, J.6
  • 65
    • 80053980485 scopus 로고    scopus 로고
    • Nanocrystals as tool to improve piroxicam dissolution rate in novel orally disintegrating tablets
    • Lai F, Pini E, Angioni G, Manca ML, Perricci J, Sinico C, et al. Nanocrystals as tool to improve piroxicam dissolution rate in novel orally disintegrating tablets. Eur J Pharm Biopharm. 2011;793:552-8.
    • (2011) Eur J Pharm Biopharm , vol.793 , pp. 552-558
    • Lai, F.1    Pini, E.2    Angioni, G.3    Manca, M.L.4    Perricci, J.5    Sinico, C.6
  • 66
    • 38749119045 scopus 로고    scopus 로고
    • Effect of arginine hydrochloride and hydroxypropyl cellulose as stabilizers on the physical stability of high drug loading nanosuspensions of a poorly soluble compound
    • Ain-Ai A, Gupta PK. Effect of arginine hydrochloride and hydroxypropyl cellulose as stabilizers on the physical stability of high drug loading nanosuspensions of a poorly soluble compound. Int J Pharm. 2008;3511-2:282-8.
    • (2008) Int J Pharm , vol.3511 , Issue.2 , pp. 282-288
    • Ain-Ai, A.1    Gupta, P.K.2
  • 67
    • 33745617678 scopus 로고    scopus 로고
    • Surface functionalized alumina nanoparticle filled polymeric nanocomposites with enhanced mechanical properties
    • Guo Z, Pereira T, Choi O, Wang Y, Hahn HT. Surface functionalized alumina nanoparticle filled polymeric nanocomposites with enhanced mechanical properties. J Mater Chem. 2006;166:2800-8.
    • (2006) J Mater Chem , vol.166 , pp. 2800-2808
    • Guo, Z.1    Pereira, T.2    Choi, O.3    Wang, Y.4    Hahn, H.T.5
  • 68
    • 61349095957 scopus 로고    scopus 로고
    • Development of an oral rutin nanocrystal formulation
    • Mauludin R, Müller RH, Keck CM. Development of an oral rutin nanocrystal formulation. Int J Pharm. 2009;3701-2:202-9.
    • (2009) Int J Pharm , vol.3701 , Issue.2 , pp. 202-209
    • Mauludin, R.1    Müller, R.H.2    Keck, C.M.3
  • 69
    • 84861098821 scopus 로고    scopus 로고
    • Generation of wear during the production of drug nanosuspensions by wet media milling
    • Juhnke M, Märtin D, John E. Generation of wear during the production of drug nanosuspensions by wet media milling. Eur J Pharm Biopharm. 2012;811:214-22.
    • (2012) Eur J Pharm Biopharm , vol.811 , pp. 214-222
    • Juhnke, M.1    Märtin, D.2    John, E.3
  • 70
    • 54349125120 scopus 로고    scopus 로고
    • Production and in vitro characterization of solid dosage form incorporating drug nanoparticles
    • Basa S, Muniyappan T, Karatgi P, Prabhu R, Pillai R. Production and in vitro characterization of solid dosage form incorporating drug nanoparticles. Drug Dev Ind Pharm. 2008;3411:1209-18.
    • (2008) Drug Dev Ind Pharm , vol.3411 , pp. 1209-1218
    • Basa, S.1    Muniyappan, T.2    Karatgi, P.3    Prabhu, R.4    Pillai, R.5
  • 72
    • 51649091116 scopus 로고    scopus 로고
    • Conversion of nanosuspensions into dry powders by spray drying: A case study
    • Chaubal MV, Popescu C. Conversion of nanosuspensions into dry powders by spray drying: a case study. Pharm Res. 2008;2510:2302-8.
    • (2008) Pharm Res , vol.2510 , pp. 2302-2308
    • Chaubal, M.V.1    Popescu, C.2
  • 73
    • 77955980572 scopus 로고    scopus 로고
    • Effective polymeric dispersants for vacuum, convection and freeze drying of drug nanosuspensions
    • Kim S, Lee J. Effective polymeric dispersants for vacuum, convection and freeze drying of drug nanosuspensions. Int J Pharm. 2010;3971-2:218-24.
    • (2010) Int J Pharm , vol.3971 , Issue.2 , pp. 218-224
    • Kim, S.1    Lee, J.2
  • 74
    • 79957861493 scopus 로고    scopus 로고
    • Nanosizing for oral and parenteral drug delivery: A perspective on formulating poorly-water soluble compounds using wet media milling technology
    • Merisko-Liversidge E, Liversidge GG. Nanosizing for oral and parenteral drug delivery: a perspective on formulating poorly-water soluble compounds using wet media milling technology. Adv Drug Deliv Rev. 2011;636:427-40.
    • (2011) Adv Drug Deliv Rev , vol.636 , pp. 427-440
    • Merisko-Liversidge, E.1    Liversidge, G.G.2
  • 75
    • 0033790335 scopus 로고    scopus 로고
    • Freeze drying of polycaprolactone and poly d, l-lactic-glycolic nanoparticles induce minor particle size changes affecting the oral pharmacokinetics of loaded drugs
    • Saez A, Guzmán M, Molpeceres J, Aberturas MR. Freeze drying of polycaprolactone and poly d, l-lactic-glycolic nanoparticles induce minor particle size changes affecting the oral pharmacokinetics of loaded drugs. Eur J Pharm Biopharm. 2000;503:379-87.
    • (2000) Eur J Pharm Biopharm , vol.503 , pp. 379-387
    • Saez, A.1    Guzmán, M.2    Molpeceres, J.3    Aberturas, M.R.4
  • 76
    • 77955086347 scopus 로고    scopus 로고
    • Pure drug nanoparticles in tablets: What are the dissolution limitations?
    • Heng D, Ogawa K, Cutler DJ, Chan H, Raper JA, Ye L, et al. Pure drug nanoparticles in tablets: what are the dissolution limitations? J Nanopart Res. 2010;125:1743-54.
    • (2010) J Nanopart Res , vol.125 , pp. 1743-1754
    • Heng, D.1    Ogawa, K.2    Cutler, D.J.3    Chan, H.4    Raper, J.A.5    Ye, L.6
  • 77
    • 43449094630 scopus 로고    scopus 로고
    • A novel bottom-up process to produce drug nanocrystals: Controlled crystallization during freeze-drying
    • de Waard H, Hinrichs WL, Frijlink HW. A novel bottom-up process to produce drug nanocrystals: controlled crystallization during freeze-drying. J Control Release. 2008;1282:179-83.
    • (2008) J Control Release , vol.1282 , pp. 179-183
    • De Waard, H.1    Hinrichs, W.L.2    Frijlink, H.W.3
  • 78
    • 33344464389 scopus 로고    scopus 로고
    • Critical freezing rate in freeze drying nanocrystal dispersions
    • Lee J, Cheng Y. Critical freezing rate in freeze drying nanocrystal dispersions. J Control Release. 2006;1111-2:185-92.
    • (2006) J Control Release , vol.1111 , Issue.2 , pp. 185-192
    • Lee, J.1    Cheng, Y.2
  • 79
    • 34249323769 scopus 로고    scopus 로고
    • Preparation of azithromycin nanosuspensions by high pressure homogenization and its physicochemical characteristics studies
    • Zhang D, Tan T, Gao L, Zhao W, Wang P. Preparation of azithromycin nanosuspensions by high pressure homogenization and its physicochemical characteristics studies. Drug Dev Ind Pharm. 2007;335:569-75.
    • (2007) Drug Dev Ind Pharm , vol.335 , pp. 569-575
    • Zhang, D.1    Tan, T.2    Gao, L.3    Zhao, W.4    Wang, P.5
  • 80
    • 37549041747 scopus 로고    scopus 로고
    • Preparation and characterization of an oridonin nanosuspension for solubility and dissolution velocity enhancement
    • Gao L, Zhang D, Chen M, Zheng T, Wang S. Preparation and characterization of an oridonin nanosuspension for solubility and dissolution velocity enhancement. Drug Dev Ind Pharm. 2007;3312:1332-9.
    • (2007) Drug Dev Ind Pharm , vol.3312 , pp. 1332-1339
    • Gao, L.1    Zhang, D.2    Chen, M.3    Zheng, T.4    Wang, S.5
  • 81
    • 41349120910 scopus 로고    scopus 로고
    • Studies on pharmacokinetics and tissue distribution of oridonin nanosuspensions
    • Gao L, Zhang D, Chen M, Duan C, Dai W, Jia L, et al. Studies on pharmacokinetics and tissue distribution of oridonin nanosuspensions. Int J Pharm. 2008;3551-2:321-7.
    • (2008) Int J Pharm , vol.3551 , Issue.2 , pp. 321-327
    • Gao, L.1    Zhang, D.2    Chen, M.3    Duan, C.4    Dai, W.5    Jia, L.6
  • 82
    • 41949130280 scopus 로고    scopus 로고
    • Formulation of nanosuspensions of albendazole for oral administration
    • Kumar MP, Rao YM, Apte S. Formulation of nanosuspensions of albendazole for oral administration. Curr Nanosci. 2008;41:53-8.
    • (2008) Curr Nanosci , vol.41 , pp. 53-58
    • Kumar, M.P.1    Rao, Y.M.2    Apte, S.3
  • 83
    • 0033965872 scopus 로고    scopus 로고
    • Preparation of a clofazimine nanosuspension for intravenous use and evaluation of its therapeutic efficacy in murine Mycobacterium avium infection
    • Peters K, Leitzke S, Diederichs JE, Borner K, Hahn H, Müller RH, et al. Preparation of a clofazimine nanosuspension for intravenous use and evaluation of its therapeutic efficacy in murine Mycobacterium avium infection. J Antimicrob Chemother. 2000;451:77-83.
    • (2000) J Antimicrob Chemother , vol.451 , pp. 77-83
    • Peters, K.1    Leitzke, S.2    Diederichs, J.E.3    Borner, K.4    Hahn, H.5    Müller, R.H.6
  • 84
    • 34249039982 scopus 로고    scopus 로고
    • Characterization of physico-chemical properties and pharmaceutical performance of sucrose co-freeze-dried solid nanoparticulate powders of the anti-HIV agent loviride prepared by media milling
    • Van Eerdenbrugh B, Froyen L, Martens JA, Blaton N, Augustijns P, Brewster M, et al. Characterization of physico-chemical properties and pharmaceutical performance of sucrose co-freeze-dried solid nanoparticulate powders of the anti-HIV agent loviride prepared by media milling. Int J Pharm. 2007;3381-2:198-206.
    • (2007) Int J Pharm , vol.3381 , Issue.2 , pp. 198-206
    • Van Eerdenbrugh, B.1    Froyen, L.2    Martens, J.A.3    Blaton, N.4    Augustijns, P.5    Brewster, M.6
  • 85
    • 37849026020 scopus 로고    scopus 로고
    • Cogrinding enhances the oral bioavailability of EMD 57033, a poorly water soluble drug, in dogs
    • Vogt M, Vertzoni M, Kunath K, Reppas C, Dressman JB. Cogrinding enhances the oral bioavailability of EMD 57033, a poorly water soluble drug, in dogs. Eur J Pharm Biopharm. 2008;682:338-45.
    • (2008) Eur J Pharm Biopharm , vol.682 , pp. 338-345
    • Vogt, M.1    Vertzoni, M.2    Kunath, K.3    Reppas, C.4    Dressman, J.B.5
  • 86
    • 21844461846 scopus 로고    scopus 로고
    • Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of nifedipine
    • Hecq J, Deleers M, Fanara D, Vranckx H, Amighi K. Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of nifedipine. Int J Pharm. 2005;2991-2:167-77.
    • (2005) Int J Pharm , vol.2991 , Issue.2 , pp. 167-177
    • Hecq, J.1    Deleers, M.2    Fanara, D.3    Vranckx, H.4    Amighi, K.5
  • 87
    • 67349199134 scopus 로고    scopus 로고
    • Advantages of celecoxib nanosuspension formulation and transformation into tablets
    • Dolenc A, Kristl J, Baumgartner S, Planinsek O. Advantages of celecoxib nanosuspension formulation and transformation into tablets. Int J Pharm. 2009;3761-2:204-12.
    • (2009) Int J Pharm , vol.3761 , Issue.2 , pp. 204-212
    • Dolenc, A.1    Kristl, J.2    Baumgartner, S.3    Planinsek, O.4
  • 88
    • 33644820008 scopus 로고    scopus 로고
    • Spray coated pellets as carrier system for mucoadhesive drug nanocrystals
    • Möschwitzer J, Müller RH. Spray coated pellets as carrier system for mucoadhesive drug nanocrystals. Eur J Pharm Biopharm. 2006;623:282-7.
    • (2006) Eur J Pharm Biopharm , vol.623 , pp. 282-287
    • Möschwitzer, J.1    Müller, R.H.2
  • 89
    • 0035927204 scopus 로고    scopus 로고
    • An oral controlled release matrix pellet formulation containing nanocrystalline ketoprofen
    • Vergote GJ, Vervaet C, Van Driessche I, Hoste S, De Smedt S, Demeester J, et al. An oral controlled release matrix pellet formulation containing nanocrystalline ketoprofen. Int J Pharm. 2001;2191-2:81-7.
    • (2001) Int J Pharm , vol.2191 , Issue.2 , pp. 81-87
    • Vergote, G.J.1    Vervaet, C.2    Van Driessche, I.3    Hoste, S.4    De Smedt, S.5    Demeester, J.6
  • 90
    • 80054683938 scopus 로고    scopus 로고
    • Lutein nanocrystals as antioxidant formulation for oral and dermal delivery
    • Mitri K, Shegokar R, Gohla S, Anselmi C, Müller RH. Lutein nanocrystals as antioxidant formulation for oral and dermal delivery. Int J Pharm. 2011;4201:141-6.
    • (2011) Int J Pharm , vol.4201 , pp. 141-146
    • Mitri, K.1    Shegokar, R.2    Gohla, S.3    Anselmi, C.4    Müller, R.H.5
  • 91
    • 0141507950 scopus 로고    scopus 로고
    • Drug nano- and microparticles processed into solid dosage forms: Physical properties
    • Lee J. Drug nano- and microparticles processed into solid dosage forms: physical properties. J Pharm Sci. 2003;9210:2057-68.
    • (2003) J Pharm Sci , vol.9210 , pp. 2057-2068
    • Lee, J.1
  • 92
    • 0041334256 scopus 로고    scopus 로고
    • Control of the morphology of nanostructured particles prepared by the spray drying of a nanoparticle sol
    • Iskandar F, Gradon L, Okuyama K. Control of the morphology of nanostructured particles prepared by the spray drying of a nanoparticle sol. J Colloid Interface Sci. 2003;2652:296-303.
    • (2003) J Colloid Interface Sci , vol.2652 , pp. 296-303
    • Iskandar, F.1    Gradon, L.2    Okuyama, K.3
  • 93
    • 0028123747 scopus 로고
    • Assessment of the degree of disorder in crystalline solids
    • Sebhatu T, Angberg M, Ahlneck C. Assessment of the degree of disorder in crystalline solids. Int J Pharm. 1994;1012:237-47.
    • (1994) Int J Pharm , vol.1012 , pp. 237-247
    • Sebhatu, T.1    Angberg, M.2    Ahlneck, C.3
  • 94
    • 0014136951 scopus 로고
    • Deaggregation behavior of a relatively insoluble substituted benzoic acid and its sodium salt
    • Aguiar AJ, Zelmer JE, Kinkel AW. Deaggregation behavior of a relatively insoluble substituted benzoic acid and its sodium salt. J Pharm Sci. 1967;5610:1243-52.
    • (1967) J Pharm Sci , vol.5610 , pp. 1243-1252
    • Aguiar, A.J.1    Zelmer, J.E.2    Kinkel, A.W.3
  • 95
    • 0035857733 scopus 로고    scopus 로고
    • Effects of initial particle size on the tableting properties of l-lysine monohydrochloride dihydrate powder
    • Sun C, Grant DJ. Effects of initial particle size on the tableting properties of l-lysine monohydrochloride dihydrate powder. Int J Pharm. 2001;2151-2:221-8.
    • (2001) Int J Pharm , vol.2151 , Issue.2 , pp. 221-228
    • Sun, C.1    Grant, D.J.2
  • 96
    • 33746768780 scopus 로고    scopus 로고
    • Compaction behaviour and new predictive approach to the compressibility of binary mixtures of pharmaceutical excipients
    • Busignies V, Leclerc B, Porion P, Evesque P, Couarraze G, Tchoreloff P. Compaction behaviour and new predictive approach to the compressibility of binary mixtures of pharmaceutical excipients. Eur J Pharm Biopharm. 2006;641:66-74.
    • (2006) Eur J Pharm Biopharm , vol.641 , pp. 66-74
    • Busignies, V.1    Leclerc, B.2    Porion, P.3    Evesque, P.4    Couarraze, G.5    Tchoreloff, P.6
  • 98
    • 53949092998 scopus 로고    scopus 로고
    • Top-down production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products
    • Van Eerdenbrugh B, Van den Mooter G, Augustijns P. Top-down production of drug nanocrystals: nanosuspension stabilization, miniaturization and transformation into solid products. Int J Pharm. 2008;3641:64-75.
    • (2008) Int J Pharm , vol.3641 , pp. 64-75
    • Van Eerdenbrugh, B.1    Van Den Mooter, G.2    Augustijns, P.3
  • 99
    • 48849111481 scopus 로고    scopus 로고
    • Drying of crystalline drug nanosuspensions - The importance of surface hydrophobicity on dissolution behavior upon redispersion
    • Van Eerdenbrugh B, Froyen L, Van Humbeeck J, Martens JA, Augustijns P, Van den Mooter G. Drying of crystalline drug nanosuspensions - the importance of surface hydrophobicity on dissolution behavior upon redispersion. Eur J Pharm Sci. 2008;351-2:127-35.
    • (2008) Eur J Pharm Sci , vol.351 , Issue.2 , pp. 127-135
    • Van Eerdenbrugh, B.1    Froyen, L.2    Van Humbeeck, J.3    Martens, J.A.4    Augustijns, P.5    Van Den Mooter, G.6
  • 100
    • 60049090585 scopus 로고    scopus 로고
    • Design of biodegradable nanoparticles for oral delivery of doxorubicin: In vivo pharmacokinetics and toxicity studies in rats
    • Kalaria DR, Sharma G, Beniwal V, Ravi Kumar MN. Design of biodegradable nanoparticles for oral delivery of doxorubicin: in vivo pharmacokinetics and toxicity studies in rats. Pharm Res. 2009;263:492-501.
    • (2009) Pharm Res , vol.263 , pp. 492-501
    • Kalaria, D.R.1    Sharma, G.2    Beniwal, V.3    Ravi Kumar, M.N.4
  • 101
    • 5344234787 scopus 로고    scopus 로고
    • The role of solid nanoparticle technology in parenteral delivery of poorly water soluble drugs
    • Kipp JE. The role of solid nanoparticle technology in parenteral delivery of poorly water soluble drugs. Int J Pharm. 2004;2841-2:109-22.
    • (2004) Int J Pharm , vol.2841 , Issue.2 , pp. 109-122
    • Kipp, J.E.1
  • 102
    • 78650531221 scopus 로고    scopus 로고
    • SDS-coated atovaquone nanosuspensions show improved therapeutic efcacy against experimental acquired and reactivated toxoplasmosis by improving passage of gastrointestinal and blood-brain barriers
    • Shubar HM, Lachenmaier S, Heimesaat MM, Lohman U, Mauludin R, Muller RH, et al. SDS-coated atovaquone nanosuspensions show improved therapeutic efcacy against experimental acquired and reactivated toxoplasmosis by improving passage of gastrointestinal and blood-brain barriers. J Drug Target. 2011;192:114-24.
    • (2011) J Drug Target , vol.192 , pp. 114-124
    • Shubar, H.M.1    Lachenmaier, S.2    Heimesaat, M.M.3    Lohman, U.4    Mauludin, R.5    Muller, R.H.6
  • 103
    • 78649648146 scopus 로고    scopus 로고
    • Pharmaceutical nanocrystals by nanomilling: Critical process parameters, particle fracturing and stabilization method
    • Peltonen L, Hirvonen J. Pharmaceutical nanocrystals by nanomilling: critical process parameters, particle fracturing and stabilization method. J Pharm Pharmacol. 2010;6211:1569-79.
    • (2010) J Pharm Pharmacol , vol.6211 , pp. 1569-1579
    • Peltonen, L.1    Hirvonen, J.2
  • 104
    • 67349098845 scopus 로고    scopus 로고
    • Diclofenac nanosuspensions: Influence of preparation procedure and crystal form on drug dissolution behavior
    • Lai F, Sinico C, Ennas G, Marongiu F, Marongiu G, Fadda AM. Diclofenac nanosuspensions: influence of preparation procedure and crystal form on drug dissolution behavior. Int J Pharm. 2009;3731-2:124-32.
    • (2009) Int J Pharm , vol.3731 , Issue.2 , pp. 124-132
    • Lai, F.1    Sinico, C.2    Ennas, G.3    Marongiu, F.4    Marongiu, G.5    Fadda, A.M.6
  • 105
    • 57149137090 scopus 로고    scopus 로고
    • Dynamic dissolution testing to establish in vitro/in vivo correlations for montelukast sodium, a poorly soluble drug
    • Okumu A, DiMaso M, Löbenberg R. Dynamic dissolution testing to establish in vitro/in vivo correlations for montelukast sodium, a poorly soluble drug. Pharm Res. 2008;2512:2778-85.
    • (2008) Pharm Res , vol.2512 , pp. 2778-2785
    • Okumu, A.1    Dimaso, M.2    Löbenberg, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.