메뉴 건너뛰기




Volumn 14, Issue 4, 2012, Pages 677-687

Crystalline nanosuspensions as potential toxicology and clinical oral formulations for BCS II/IV Compounds

Author keywords

Bioavailability enhancement; Nanocrystals; Nanoparticles; Nanosizing; Nanosuspensions

Indexed keywords

APREPITANT; CARBENDAZIM; CILOSTAZOL; DANAZOL; EFAVIRENZ; FENOFIBRATE; GRISEOFULVIN; MACROGOL 400; MEGESTROL ACETATE; NANOPARTICLE; POLYSORBATE 80; RAPAMYCIN;

EID: 84869118853     PISSN: 15507416     EISSN: None     Source Type: Journal    
DOI: 10.1208/s12248-012-9383-0     Document Type: Article
Times cited : (66)

References (36)
  • 2
    • 84859998651 scopus 로고    scopus 로고
    • A biopharmaceutical classification-based rightfirst-Time formulation approach to reduce human pharmacokinetic variability and project cycle time from first-in-human to clinical proof-of-concept
    • Ku MS, Dulin W. A biopharmaceutical classification-based rightfirst-Time formulation approach to reduce human pharmacokinetic variability and project cycle time from first-in-human to clinical proof-of-concept. Pharm Dev Technol. 2012; 17:285-302.
    • (2012) Pharm Dev Technol , vol.17 , pp. 285-283
    • Ku, M.S.1    Dulin, W.2
  • 3
    • 0037312695 scopus 로고    scopus 로고
    • Nanosizing: A formulation approach for poorly-water-soluble compounds
    • Merisko-Liversidge E, Liversidge GG, Cooper ER. Nanosizing: a formulation approach for poorly-water-soluble compounds. Eur J Pharm Sci. 2003;18:113-20.
    • (2003) Eur J Pharm Sci , vol.18 , pp. 113-112
    • Merisko-Liversidge, E.1    Liversidge, G.G.2    Cooper, E.R.3
  • 4
    • 34548049483 scopus 로고    scopus 로고
    • Nanosizing-oral formulation development and biopharmaceutical evaluation
    • Kesisoglou F, Panmai S, Wu Y. Nanosizing-oral formulation development and biopharmaceutical evaluation. Adv Drug Deliv Rev. 2007;59:631-44.
    • (2007) Adv Drug Deliv Rev , vol.59 , pp. 631-634
    • Kesisoglou, F.1    Panmai, S.2    Wu, Y.3
  • 5
    • 79957861493 scopus 로고    scopus 로고
    • Nanosizing for oral and parenteral drug delivery: A perspective on formulating poorlywater soluble compounds using wet media milling technology
    • Merisko-Liversidge E, Liversidge GG. Nanosizing for oral and parenteral drug delivery: a perspective on formulating poorlywater soluble compounds using wet media milling technology. Adv Drug Deliv Rev. 2011;63:427-40.
    • (2011) Adv Drug Deliv Rev , vol.63 , pp. 427-424
    • Merisko-Liversidge, E.1    Liversidge, G.G.2
  • 6
    • 41949100244 scopus 로고    scopus 로고
    • Drug nanoparticles: Formulating poorly water-soluble compounds
    • Merisko-Liversidge EM, Liversidge GG. Drug nanoparticles: formulating poorly water-soluble compounds. Toxicol Pathol. 2008;36:43-8.
    • (2008) Toxicol Pathol , vol.36 , pp. 43-48
    • Merisko-Liversidge, E.M.1    Liversidge, G.G.2
  • 7
    • 77956882799 scopus 로고    scopus 로고
    • Nanocrystals: Industrially feasible multifunctional formulation technology for poorly soluble actives
    • Shegokar R, Müller RH. Nanocrystals: industrially feasible multifunctional formulation technology for poorly soluble actives. Int J Pharm. 2010;399:129-39.
    • (2010) Int J Pharm , vol.399 , pp. 129-123
    • Shegokar, R.1    Müller, R.H.2
  • 8
    • 53949092998 scopus 로고    scopus 로고
    • Topdown production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products
    • Van Eerdenbrugh B, Van den Mooter G, Augustijns P. Topdown production of drug nanocrystals: nanosuspension stabilization, miniaturization and transformation into solid products. Int J Pharm. 2008;364:64-75.
    • (2008) Int J Pharm , vol.364 , pp. 64-67
    • Van Eerdenbrugh, B.1    Van Den Mooter, G.2    Augustijns, P.3
  • 9
    • 0035292910 scopus 로고    scopus 로고
    • Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract
    • Horter D, Dressman JB. Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract. Adv Drug Deliv Rev. 2001;46:75-87.
    • (2001) Adv Drug Deliv Rev , vol.46 , pp. 75-78
    • Horter, D.1    Dressman, J.B.2
  • 10
    • 0031913402 scopus 로고    scopus 로고
    • Dissolution testing as a prognostic tool for oral drug adsorption: Immediate release dosage forms
    • Dressman JB, Amidon GL, Reppas C, Shah VP. Dissolution testing as a prognostic tool for oral drug adsorption: immediate release dosage forms. Pharm Res. 1998;15:11-22.
    • (1998) Pharm Res , vol.15 , pp. 11-12
    • Dressman, J.B.1    Amidon, G.L.2    Reppas, C.3    Shah, V.P.4
  • 11
    • 0029023516 scopus 로고
    • The effect of particle size and shape on the surface specific dissolution rate of micronized practically insoluble drugs
    • Mosharraf M, Nystrom C. The effect of particle size and shape on the surface specific dissolution rate of micronized practically insoluble drugs. Int J Pharm. 1995;122:35-47.
    • (1995) Int J Pharm , vol.122 , pp. 35-34
    • Mosharraf, M.1    Nystrom, C.2
  • 12
    • 84857502649 scopus 로고    scopus 로고
    • A formulation strategy for gamma secretase inhibitor elnd006, a bcs class ii compound: Development of a nanosuspension formulation with improved oral bioavailability and reduced food effects in dogs
    • Quinn K, Gullapalli RP, Merisko-Liversidge E, Goldbach E, Wong A, Liversidge GG, et al. A formulation strategy for gamma secretase inhibitor ELND006, a BCS class II compound: development of a nanosuspension formulation with improved oral bioavailability and reduced food effects in dogs. J Pharm Sci. 2012;101:1462-74.
    • (2012) J Pharm Sci , vol.101 , pp. 1462-1467
    • Quinn, K.1    Gullapalli, R.P.2    Merisko-Liversidge, E.3    Goldbach, E.4    Wong, A.5    Liversidge, G.G.6
  • 13
    • 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
    • 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;285:135-46.
    • (2004) Int J Pharm , vol.285 , pp. 135-134
    • Wu, Y.1    Loper, A.2    Landis, E.3    Hettrick, L.4    Novak, L.5    Lynn, K.6
  • 14
    • 79959317121 scopus 로고    scopus 로고
    • Investigation of nanosized crystalline form to improve the oral bioavailability of poorly water soluble cilostazol
    • Miao X, Sun C, Jiang T, Zheng L, Wang T, Wang S. Investigation of nanosized crystalline form to improve the oral bioavailability of poorly water soluble cilostazol. J Pharm Pharm Sci. 2011;14 (2):196-214.
    • (2011) J Pharm Pharm Sci , vol.14 , Issue.2 , pp. 196-192
    • Miao, X.1    Sun, C.2    Jiang, T.3    Zheng, L.4    Wang, T.5    Wang, S.6
  • 15
    • 0023709168 scopus 로고    scopus 로고
    • Physiochemical aspects of drug release. Viii. The relation between particle size and surface specific dissolution rate in agitated suspensions
    • Nystrom C, Bisrat M. Physiochemical aspects of drug release. VIII. The relation between particle size and surface specific dissolution rate in agitated suspensions. Int J Pharm. 1998;47:223-31.
    • (1998) Int J Pharm , vol.47 , pp. 223-223
    • Nystrom, C.1    Bisrat, M.2
  • 16
    • 0342897023 scopus 로고    scopus 로고
    • Nanosuspensions for the formulation of poorly soluble drugs i. Preparation by a size-reduction technique
    • Muller RH, Peters K. Nanosuspensions for the formulation of poorly soluble drugs I. Preparation by a size-reduction technique. Int J Pharm. 1998;160:229-37.
    • (1998) Int J Pharm , vol.160 , pp. 229-223
    • Muller, R.H.1    Peters, K.2
  • 17
    • 77649191330 scopus 로고    scopus 로고
    • Possible reduction of effective thickness of intestinal unstirred water layer by particle drifting effect
    • Sugano K. Possible reduction of effective thickness of intestinal unstirred water layer by particle drifting effect. Int J Pharm. 2010;387:103-9.
    • (2010) Int J Pharm , vol.387 , pp. 103-109
    • Sugano, K.1
  • 18
    • 67349159812 scopus 로고    scopus 로고
    • Theoretical investigation of passive intestinal membrane permeability using monte carlo method to generate druglike molecule population
    • Sugano K. Theoretical investigation of passive intestinal membrane permeability using Monte Carlo method to generate druglike molecule population. Int J Pharm. 2009;373:55-61.
    • (2009) Int J Pharm , vol.373 , pp. 55-56
    • Sugano, K.1
  • 19
    • 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;25 (10):2302-8.
    • (2008) Pharm Res , vol.25 , Issue.10 , pp. 2302-2308
    • Chaubal, M.V.1    Popescu, C.2
  • 21
    • 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
    • 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;111:56-64.
    • (2006) J Control Release , vol.111 , pp. 56-56
    • Jinno, J.1    Kamada, N.2    Miyake, M.3    Yamada, K.4    Mukai, T.5    Odomi, M.6
  • 22
    • 77955656443 scopus 로고    scopus 로고
    • Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans
    • Shono Y, Jantratid E, Kesisoglou F, Reppas C, Dressmam JB. Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans. Eur J Pharm Biopharm. 2010;76:95-104.
    • (2010) Eur J Pharm Biopharm , vol.76 , pp. 95-91
    • Shono, Y.1    Jantratid, E.2    Kesisoglou, F.3    Reppas, C.4    Dressmam, J.B.5
  • 23
    • 0037227770 scopus 로고    scopus 로고
    • Carbendazim: Disposition, cellular permeability, metabolite identification, and pharmacokinetic comparison with its nanoparticle
    • Jia L, Wong H, Wang Y, Garza M, Weitman SD. Carbendazim: disposition, cellular permeability, metabolite identification, and pharmacokinetic comparison with its nanoparticle. J Pharm Sci. 2003;92:161-72.
    • (2003) J Pharm Sci , vol.92 , pp. 161-167
    • Jia, L.1    Wong, H.2    Wang, Y.3    Garza, M.4    Weitman, S.D.5
  • 24
    • 33750089277 scopus 로고    scopus 로고
    • Preparation and in vitro/in vivo evaluation of nano-sized crystals for dissolution rate enhancement of ucb-35440-3, a highly dosed poorly water-soluble weak base
    • Hecq J, Deleers M, Fanara D, Vranckx H, Boulanger P, Le Lamer S, et al. Preparation and in vitro/in vivo evaluation of nano-sized crystals for dissolution rate enhancement of ucb-35440-3, a highly dosed poorly water-soluble weak base. Eur J Pharm Biopharm. 2006;64:360-8.
    • (2006) Eur J Pharm Biopharm , vol.64 , pp. 360-368
    • Hecq, J.1    Deleers, M.2    Fanara, D.3    Vranckx, H.4    Boulanger, P.5    Le Lamer, S.6
  • 25
    • 71049183092 scopus 로고    scopus 로고
    • Particle size reduction for improvement of oral absorption of the poorly soluble drug ug558 in rats during early development
    • Sigfridsson K, Lundqvist AJ, Strimfors M. Particle size reduction for improvement of oral absorption of the poorly soluble drug UG558 in rats during early development. Drug Dev Ind Pharm. 2009;35:1479-86.
    • (2009) Drug Dev Ind Pharm , vol.35 , pp. 1479-1478
    • Sigfridsson, K.1    Lundqvist, A.J.2    Strimfors, M.3
  • 26
    • 11144354093 scopus 로고    scopus 로고
    • Influence of physicochemical properties and intestinal region on the absorption of 3-fluoro-2-pyrimidylmethyl 3-(2,2-difluoro-2-(2-pyridyl) ethylamino)-6-chloropyrazin-2-one-1-Acetamide, a water insoluble thrombin inhibitor, in dog
    • Euler D, Frech P, Karki S, Cowden C, Pearce G, Mehta P, et al. Influence of physicochemical properties and intestinal region on the absorption of 3-fluoro-2-pyrimidylmethyl 3-(2,2-difluoro-2-(2-pyridyl) ethylamino)-6- chloropyrazin-2-one-1-Acetamide, a water insoluble thrombin inhibitor, in dog. Int J Pharm. 2004;275:19-27.
    • (2004) Int J Pharm , vol.275 , pp. 19-12
    • Euler, D.1    Frech, P.2    Karki, S.3    Cowden, C.4    Pearce, G.5    Mehta, P.6
  • 27
    • 0036689390 scopus 로고    scopus 로고
    • Effect of nanonization on absorption of 301029: Ex vivo and in vivo pharmacokinetic correlations determined by liquid chromatography/mass spectrometry
    • Jia L, Wong H, Cerna C, Weitman SD. Effect of nanonization on absorption of 301029: ex vivo and in vivo pharmacokinetic correlations determined by liquid chromatography/mass spectrometry. Pharm Res. 2002;19:1091-6.
    • (2002) Pharm Res , vol.19 , pp. 1091-1096
    • Jia, L.1    Wong, H.2    Cerna, C.3    Weitman, S.D.4
  • 28
    • 0027243792 scopus 로고
    • Improved oral absorption of a poorly watersoluble drug, ho-221, by wet-bead milling producing particles in submicron region
    • Kondo N, Iwao T, Masuda H, Yamanouchi K, Ishihara Y, Yamada N, et al. Improved oral absorption of a poorly watersoluble drug, HO-221, by wet-bead milling producing particles in submicron region. Chem Pharm Bull (Tokyo). 1993;41:737-40.
    • (1993) Chem Pharm Bull (Tokyo , vol.41 , pp. 737-734
    • Kondo, N.1    Iwao, T.2    Masuda, H.3    Yamanouchi, K.4    Ishihara, Y.5    Yamada, N.6
  • 29
    • 0029080002 scopus 로고
    • Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs
    • LiversidgeGG, CundyKC. 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;125:91-7.
    • (1995) Int J Pharm , Issue.125 , pp. 91-97
    • Liversidge, G.G.1    Cundy, K.C.2
  • 30
    • 61349191553 scopus 로고    scopus 로고
    • Enhancement of oral bioavailability of an hivattachment inhibitor by nanosizing and amorphous formulation approaches
    • Fakes MG, Vakkalagadda BJ, Qian F, Desikan S, Gandhi RB, Lai C, et al. Enhancement of oral bioavailability of an HIVattachment inhibitor by nanosizing and amorphous formulation approaches. Int J Pharm. 2009;370:167-74.
    • (2009) Int J Pharm , vol.370 , pp. 167-167
    • Fakes, M.G.1    Vakkalagadda, B.J.2    Qian, F.3    Desikan, S.4    Gandhi, R.B.5    Lai, C.6
  • 31
    • 3943083748 scopus 로고    scopus 로고
    • Wyeth Pharmaceuticals Inc. Philadelphia: Wyeth Pharmaceuticals
    • Wyeth Pharmaceuticals, Inc.Rapamune(R) prescribing information. Philadelphia: Wyeth Pharmaceuticals; 2006.
    • (2006) Rapamune(R) Prescribing Information
  • 33
    • 33847094347 scopus 로고    scopus 로고
    • Par Pharmaceutical Companies Inc. Woodcliff: Par Pharmaceutical Companies
    • Par Pharmaceutical Companies, Inc. Megace(R) ES prescribing information. Woodcliff: Par Pharmaceutical Companies; 2005.
    • (2005) Megace(R) ES Prescribing Information
  • 35
    • 34548027773 scopus 로고    scopus 로고
    • Abbott Laboratories. Abbott Park: Abbott Laboratories
    • Abbott Laboratories. TriCor(R) prescribing information. Abbott Park: Abbott Laboratories; 2004.
    • (2004) TriCor(R) Prescribing Information
  • 36
    • 84869123618 scopus 로고    scopus 로고
    • First Horizon Pharmaceutical Corporation. Roswell: First Horizon Pharmaceutical Corporation
    • First Horizon Pharmaceutical Corporation. TriglideTM prescribing information. Roswell: First Horizon Pharmaceutical Corporation; 2005.
    • (2005) TriglideTM Prescribing Information


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.