-
1
-
-
67449119172
-
Development of a longacting injectable formulation with nanoparticles of rilpivirine (TMC278) for HIV treatment
-
Baert L, van 't Klooster G, Dries W, Fran?is M, Wouters A, Basstanie E, Iterbeke K, Stappers F, Stevens P, Schueller L, Van Remoortere P, Kraus G, Wigerinck P, Rosier J. (2009). Development of a longacting injectable formulation with nanoparticles of rilpivirine (TMC278) for HIV treatment. Eur J Pharm Biopharm, 72, 502-508.
-
(2009)
Eur. J. Pharm. Biopharm.
, vol.72
, pp. 502-508
-
-
Baert, L.1
Van't Klooster, G.2
Dries, W.3
Franis, M.4
Wouters, A.5
Basstanie, E.6
Iterbeke, K.7
Stappers, F.8
Stevens, P.9
Schueller, L.10
Van Remoortere, P.11
Kraus, G.12
Wigerinck, P.13
Rosier, J.14
-
2
-
-
52949128719
-
Comparison of nanosuspensions and hydroxypropyl-beta-cyclodextrin complex of melarsoprol: Pharmacokinetics and tissue distribution in mice
-
Ben Zirar S, Astier A, Muchow M, Gibaud S. (2008). Comparison of nanosuspensions and hydroxypropyl-beta-cyclodextrin complex of melarsoprol: pharmacokinetics and tissue distribution in mice. Eur J Pharm Biopharm, 70, 649-656.
-
(2008)
Eur J Pharm Biopharm
, vol.70
, pp. 649-656
-
-
Ben Zirar, S.1
Astier, A.2
Muchow, M.3
Gibaud, S.4
-
3
-
-
0032903302
-
HPLC determination of clofazimine in tissues and serum of mice after intravenous administration of nanocrystalline or liposomal formulations
-
Borner K, Hartwig H, Leitzke S, Hahn H, Müler RH, Ehlers S. (1999). HPLC determination of clofazimine in tissues and serum of mice after intravenous administration of nanocrystalline or liposomal formulations. Int J Antimicrob Agents, 11, 75-79.
-
(1999)
Int. J. Antimicrob Agents
, vol.11
, pp. 75-79
-
-
Borner, K.1
Hartwig, H.2
Leitzke, S.3
Hahn, H.4
Müler, R.H.5
Ehlers, S.6
-
4
-
-
77955052417
-
Miconazole nanosuspensions: Influence of formulation variables on particle size reduction and physical stability
-
Cerdeira AM, Mazzotti M, Gander B. (2010). Miconazole nanosuspensions: Influence of formulation variables on particle size reduction and physical stability. Int J Pharm, 396, 210-218.
-
(2010)
Int. J. Pharm.
, vol.396
, pp. 210-218
-
-
Cerdeira, A.M.1
Mazzotti, M.2
Gander, B.3
-
5
-
-
79953685905
-
Nanonization strategies for poorly water-soluble drugs
-
Chen H, Khemtong C, Yang X, Chang X, Gao J. (2011). Nanonization strategies for poorly water-soluble drugs. Drug Discov Today, 16, 354-360.
-
(2011)
Drug Discov Today
, vol.16
, pp. 354-360
-
-
Chen, H.1
Khemtong, C.2
Yang, X.3
Chang, X.4
Gao, J.5
-
6
-
-
67349138612
-
Two-stage microfluidization combined with ultrafiltration treatment for chitosan mass production and molecular weight manipulation
-
Chen RH, Tsai ML, Tseng LZ. (2009). Two-stage microfluidization combined with ultrafiltration treatment for chitosan mass production and molecular weight manipulation. Carbohyd Polym, 77, 767-772.
-
(2009)
Carbohyd Polym
, vol.77
, pp. 767-772
-
-
Chen, R.H.1
Tsai, M.L.2
Tseng, L.Z.3
-
7
-
-
0034110573
-
Synthesis of nanoparticles with novel technology: High-gravity reactive precipitation
-
Chen JF, Wang YH, Guo F, Wang XM, Zheng C. (2000). Synthesis of nanoparticles with novel technology: high-gravity reactive precipitation. Ind Eng Chem Res, 39, 948-954.
-
(2000)
Ind. Eng. Chem. Res.
, vol.39
, pp. 948-954
-
-
Chen, J.F.1
Wang, Y.H.2
Guo, F.3
Wang, X.M.4
Zheng, C.5
-
8
-
-
51349121937
-
A facile nanoaggregation strategy for oral delivery of hydrophobic drugs by utilizing acid-base neutralization reactions
-
Chen H, Wan J, Wang Y, Mou D, Liu H, Xu H, Yang X. (2008). A facile nanoaggregation strategy for oral delivery of hydrophobic drugs by utilizing acid-base neutralization reactions. Nanotechnology, 19, 375104.
-
(2008)
Nanotechnology
, vol.19
, pp. 375104
-
-
Chen, H.1
Wan, J.2
Wang, Y.3
Mou, D.4
Liu, H.5
Xu, H.6
Yang, X.7
-
9
-
-
0030148294
-
Interaction of macro-and micromixing on particle size distribution in reaction precipitation
-
Chen JF, Zheng C, Chen GT. (1996). Interaction of macro-and micromixing on particle size distribution in reaction precipitation. Chem Eng Sci, 51, 1957-1966.
-
(1996)
Chem. Eng. Sci.
, vol.51
, pp. 1957-1966
-
-
Chen, J.F.1
Zheng, C.2
Chen, G.T.3
-
10
-
-
0348048800
-
Feasibility of preparing nanodrugs by high-gravity reactive precipitation
-
Chen JF, Zhou MY, Shao L, Wang YY, Yun J, Chew NY, Chan HK. (2004). Feasibility of preparing nanodrugs by high-gravity reactive precipitation. Int J Pharm, 269, 267-274.
-
(2004)
Int. J. Pharm.
, vol.269
, pp. 267-274
-
-
Chen, J.F.1
Zhou, M.Y.2
Shao, L.3
Wang, Y.Y.4
Yun, J.5
Chew, N.Y.6
Chan, H.K.7
-
11
-
-
84863296052
-
Synthesis of ultrafine calcium carbonate
-
Patent No ZL95105343.4
-
Chen JF, Zhou XM, Wang YH, Zheng C. (1998). Synthesis of ultrafine calcium carbonate. Chinese Patent No. ZL95105343.4.
-
(1998)
Chinese
-
-
Chen, J.F.1
Zhou, X.M.2
Wang, Y.H.3
Zheng, C.4
-
12
-
-
84863296233
-
Ultrafine particle synthesis by high-gravity reactive precipitation
-
Patent No.95105344.2
-
Chen JF, Zhou XM, Zheng C. (1995). Ultrafine particle synthesis by high-gravity reactive precipitation. Chinese Patent No. 95105344.2.
-
(1995)
Chinese
-
-
Chen, J.F.1
Zhou, X.M.2
Zheng, C.3
-
13
-
-
59949091288
-
Evaluation of aerosol delivery of nanosuspension for pre-clinical pulmonary drug delivery
-
Chiang PC, Alsup JW, Lai Y, Hu Y, Heyde BR, Tung D. (2009). Evaluation of Aerosol Delivery of Nanosuspension for Pre-clinical Pulmonary Drug Delivery. Nanoscale Res Lett, 4, 254-261.
-
(2009)
Nanoscale Res. Lett.
, vol.4
, pp. 254-261
-
-
Chiang, P.C.1
Alsup, J.W.2
Lai, Y.3
Hu, Y.4
Heyde, B.R.5
Tung, D.6
-
15
-
-
67349199134
-
Advantages of celecoxib nanosuspension formulation and transformation into tablets
-
Dolenc A, Kristl J, Baumgartner S, Planinsek O. (2009). Advantages of celecoxib nanosuspension formulation and transformation into tablets. Int J Pharm, 376, 204-212.
-
(2009)
Int. J. Pharm.
, vol.376
, pp. 204-212
-
-
Dolenc, A.1
Kristl, J.2
Baumgartner, S.3
Planinsek, O.4
-
16
-
-
61349191553
-
Enhancement of oral bioavailability of an HIV-attachment inhibitor by nanosizing and amorphous formulation approaches
-
Fakes MG, Vakkalagadda BJ, Qian F, Desikan S, Gandhi RB, Lai C, Hsieh A, Franchini MK, Toale H, Brown J. (2009). Enhancement of oral bioavailability of an HIV-attachment inhibitor by nanosizing and amorphous formulation approaches. Int J Pharm, 370, 167-174.
-
(2009)
Int. J. Pharm.
, vol.370
, pp. 167-174
-
-
Fakes, M.G.1
Vakkalagadda, B.J.2
Qian, F.3
Desikan, S.4
Gandhi, R.B.5
Lai, C.6
Hsieh, A.7
Franchini, M.K.8
Toale, H.9
Brown, J.10
-
17
-
-
79953235959
-
Growth inhibition and induction of apoptosis in MCF-7 breast cancer cells by oridonin nanosuspension
-
Feng FF, Zhang DR, Tian KL, Lou HY, Qi XL, Wang YC, Duan CX, Jia LJ, Wang FH, Liu Y, Zhang Q. (2011). Growth inhibition and induction of apoptosis in MCF-7 breast cancer cells by oridonin nanosuspension. Drug Deliv, 18, 265-271.
-
(2011)
Drug Deliv.
, vol.18
, pp. 265-271
-
-
Feng, F.F.1
Zhang, D.R.2
Tian, K.L.3
Lou, H.Y.4
Qi, X.L.5
Wang, Y.C.6
Duan, C.X.7
Jia, L.J.8
Wang, F.H.9
Liu, Y.10
Zhang, Q.11
-
18
-
-
0012248471
-
Higee-A status report
-
Fowler R. (1989). Higee-a status report. Chem Eng, 35, 456-473.
-
(1989)
Chem. Eng.
, vol.35
, pp. 456-473
-
-
Fowler, R.1
-
19
-
-
64249128053
-
Formulation development and evaluation of metronidazole magnetic nanosuspension as a magnetic-targeted and polymericcontrolled drug delivery system
-
Formulation development and evaluation of metronidazole magnetic nanosuspension as a magnetic-targeted and polymericcontrolled drug delivery system. J Magn Magn Mater, 321, 1580-1585.
-
J. Magn. Magn. Mater.
, vol.321
, pp. 1580-1585
-
-
-
20
-
-
77956398535
-
Preparation, characterization, pharmacokinetics, and tissue distribution of curcumin nanosuspension with TPGS as stabilizer
-
Gao Y, Li Z, Sun M, Li H, Guo C, Cui J, Li A, Cao F, Xi Y, Lou H, Zhai G. (2010). Preparation, characterization, pharmacokinetics, and tissue distribution of curcumin nanosuspension with TPGS as stabilizer. Drug Dev Ind Pharm, 36, 1225-1234.
-
(2010)
Drug Dev. Ind. Pharm.
, vol.36
, pp. 1225-1234
-
-
Gao, Y.1
Li, Z.2
Sun, M.3
Li, H.4
Guo, C.5
Cui, J.6
Li, A.7
Cao, F.8
Xi, Y.9
Lou, H.10
Zhai, G.11
-
21
-
-
41349120910
-
Studies on pharmacokinetics and tissue distribution of oridonin nanosuspensions
-
Gao L, Zhang D, Chen M, Duan C, Dai W, Jia L, Zhao W. (2008b). Studies on pharmacokinetics and tissue distribution of oridonin nanosuspensions. Int J Pharm, 355, 321-327.
-
(2008)
Int. J. Pharm.
, vol.355
, pp. 321-327
-
-
Gao, L.1
Zhang, D.2
Chen, M.3
Duan, C.4
Dai, W.5
Jia, L.6
Zhao, W.7
-
22
-
-
0343340404
-
Synchronous visual and RTD study on liquid ?ow inrotating packed-bed contactor
-
Guo K, Guo F, Feng YD, Chen JF, Zheng C, Gardner NC. (2000). Synchronous visual and RTD study on liquid ?ow inrotating packed-bed contactor. Chem Eng Sci, 55, 1699-1706.
-
(2000)
Chem. Eng. Sci.
, vol.55
, pp. 1699-1706
-
-
Guo, K.1
Guo, F.2
Feng, Y.D.3
Chen, J.F.4
Zheng, C.5
Gardner, N.C.6
-
23
-
-
1142303337
-
What is the true solubility advantage for amorphous pharmaceuticals?
-
Hancock BC, Parks M. (2000). What is the true solubility advantage for amorphous pharmaceuticals? Pharm Res, 17, 397-404.
-
(2000)
Pharm. Res.
, vol.17
, pp. 397-404
-
-
Hancock, B.C.1
Parks, M.2
-
24
-
-
33750089277
-
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, Amighi K. (2006). 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, 64, 360-368.
-
(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
Amighi, K.7
-
25
-
-
0035910873
-
Production and characterization of mucoadhesive nanosuspensions for the formulation of bupravaquone
-
Jacobs C, Kayser O, Müler RH. (2001). Production and characterization of mucoadhesive nanosuspensions for the formulation of bupravaquone. Int J Pharm, 214, 3-7.
-
(2001)
Int. J. Pharm.
, vol.214
, pp. 3-7
-
-
Jacobs, C.1
Kayser, O.2
Müler, R.H.3
-
26
-
-
34447254990
-
Nanosuspension as an ophthalmic delivery system for certain glucocorticoid drugs
-
Kassem MA, Abdel Rahman AA, Ghorab MM, Ahmed MB, Khalil RM. (2007). Nanosuspension as an ophthalmic delivery system for certain glucocorticoid drugs. Int J Pharm, 340, 126-133.
-
(2007)
Int. J. Pharm.
, vol.340
, pp. 126-133
-
-
Kassem, M.A.1
Abdel Rahman, A.A.2
Ghorab, M.M.3
Ahmed, M.B.4
Khalil, R.M.5
-
27
-
-
0033970268
-
Nanosuspensions for the formulation of aphidicolin to improve drug targeting effects against leishmania infected macrophages
-
Kayser O. (2000). Nanosuspensions for the formulation of aphidicolin to improve drug targeting effects against leishmania infected macrophages. Int J Pharm, 196, 253-256.
-
(2000)
Int. J. Pharm.
, vol.196
, pp. 253-256
-
-
Kayser, O.1
-
28
-
-
0035910888
-
A new approach for targeting to Cryptosporidium parvum using mucoadhesive nanosuspensions: Research and applications
-
Kayser O. (2001). A new approach for targeting to Cryptosporidium parvum using mucoadhesive nanosuspensions: research and applications. Int J Pharm, 214, 83-85.
-
(2001)
Int. J. Pharm.
, vol.214
, pp. 83-85
-
-
Kayser, O.1
-
29
-
-
0037453179
-
Formulation of amphotericin B as nanosuspension for oral administration
-
Kayser O, Olbrich C, Yardley V, Kiderlen AF, Croft SL. (2003). Formulation of amphotericin B as nanosuspension for oral administration. Int J Pharm, 254, 73-75.
-
(2003)
Int. J. Pharm.
, vol.254
, pp. 73-75
-
-
Kayser, O.1
Olbrich, C.2
Yardley, V.3
Kiderlen, A.F.4
Croft, S.L.5
-
30
-
-
0034756945
-
Biodegradable nanoparticles for targeted drug delivery in treatment of inflammatory bowel disease
-
Kawashima Y, Lehr CM. (2001). Biodegradable nanoparticles for targeted drug delivery in treatment of inflammatory bowel disease. J Pharmacol Exp Ther, 299, 775-781.
-
(2001)
J. Pharmacol Exp Ther
, vol.299
, pp. 775-781
-
-
Kawashima, Y.1
Lehr, C.M.2
-
31
-
-
34548049483
-
Nanosizing-oral formulation development and biopharmaceutical evaluation
-
Kesisoglou F, Panmai S, Wu Y. (2007). Nanosizing-oral formulation development and biopharmaceutical evaluation. Adv Drug Deliv Rev, 59, 631-644.
-
(2007)
Adv Drug Deliv Rev
, vol.59
, pp. 631-644
-
-
Kesisoglou, F.1
Panmai, S.2
Wu, Y.3
-
32
-
-
5344234787
-
The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugs
-
Kipp JE. (2004). The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugs. Int J Pharm, 284, 109-122.
-
(2004)
Int. J. Pharm.
, vol.284
, pp. 109-122
-
-
Kipp, J.E.1
-
33
-
-
33645030096
-
Preparation and evaluation of nanosuspensions for enhancing the dissolution of poorly soluble drugs
-
Kocbek P, Baumgartner S, Kristl J. (2006). Preparation and evaluation of nanosuspensions for enhancing the dissolution of poorly soluble drugs. Int J Pharm, 312, 179-186.
-
(2006)
Int. J. Pharm.
, vol.312
, pp. 179-186
-
-
Kocbek, P.1
Baumgartner, S.2
Kristl, J.3
-
34
-
-
67349199134
-
Advantages of celecoxib nanosuspension formulation and transformation into tablets
-
Kristl J, Dolenc A, Baumgartner S, Planinsek O. (2009). Advantages of celecoxib nanosuspension formulation and transformation into tablets. Int J Pharm, 376, 204-212.
-
(2009)
Int. J. Pharm.
, vol.376
, pp. 204-212
-
-
Kristl, J.1
Dolenc, A.2
Baumgartner, S.3
Planinsek, O.4
-
35
-
-
67349098845
-
Diclofenac nanosuspensions: influence of preparation procedure nd crystal form on drug dissolution behaviour
-
Lai F, Sinico C, Ennas G, Marongiu F, Marongiu G, Fadda AM. (2009). Diclofenac nanosuspensions: influence of preparation procedure nd crystal form on drug dissolution behaviour. Int J Pharm, 373, 124-132.
-
(2009)
Int. J. Pharm.
, vol.373
, pp. 124-132
-
-
Lai, F.1
Sinico, C.2
Ennas, G.3
Marongiu, F.4
Marongiu, G.5
Fadda, A.M.6
-
36
-
-
0034756945
-
Biodegradable nanoparticles for targeted drug delivery in treatment of inflammatory bowel disease
-
Lamprecht A, Ubrich N, Yamamoto H, Schäer U, Takeuchi H, Maincent P, Kawashima Y, Lehr CM. (2001). Biodegradable nanoparticles for targeted drug delivery in treatment of inflammatory bowel disease. J Pharmacol Exp Ther, 299, 775-781.
-
(2001)
J. Pharmacol Exp Ther
, vol.299
, pp. 775-781
-
-
Lamprecht, A.1
Ubrich, N.2
Yamamoto, H.3
Schäer, U.4
Takeuchi, H.5
Maincent, P.6
Kawashima, Y.7
Lehr, C.M.8
-
37
-
-
64249128053
-
Formulation development and evaluation of metronidazole magnetic nanosuspension as a magnetic-targeted and polymeric-controlled drug delivery system
-
Latha S, Selvamani P, Kumar CS, Sharavanan P, Suganya G, Beniwal VS, Rao PR. (2009). Formulation development and evaluation of metronidazole magnetic nanosuspension as a magnetic-targeted and polymeric-controlled drug delivery system. J Mang Mang Mater, 321, 1580-1585.
-
(2009)
J. Mang Mang Mater
, vol.321
, pp. 1580-1585
-
-
Latha, S.1
Selvamani, P.2
Kumar, C.S.3
Sharavanan, P.4
Suganya, G.5
Beniwal, V.S.6
Rao, P.R.7
-
38
-
-
33344464389
-
Critical freezing rate in freeze drying nanocrystal dispersions
-
Lee J, Cheng Y. (2006). Critical freezing rate in freeze drying nanocrystal dispersions. J Control Release, 111, 185-192.
-
(2006)
J. Control Release
, vol.111
, pp. 185-192
-
-
Lee, J.1
Cheng, Y.2
-
39
-
-
84863259961
-
Water-insoluble drug formation. interpharm press
-
Liu R, ed.). Particle size reduction
-
Lee RW, Mcshane J, Shaw JM, Wood RW. (2000). Particle size reduction. In: Liu R, ed. Water-Insoluble Drug Formation. Interpharm Press, Buffalo Grove, 455-492.
-
(2000)
Buffalo Grove
, pp. 455-492
-
-
Lee, R.W.1
McShane, J.2
Shaw, J.M.3
Wood, R.W.4
-
41
-
-
68649106338
-
-
Lou H, Zhang X, Gao L, Feng F, Wang J, Wei X, Yu Z, Zhang D, Zhang Q. (2009). In vitro and in vivo antitumor activity of oridonin nanosuspension. Int J Pharm, 379, 181-186.
-
(2009)
Vitro and in Vivo Antitumor Activity of Oridonin Nanosuspension. Int J Pharm
, vol.379
, pp. 181-186
-
-
Lou, H.1
Zhang, X.2
Gao, L.3
Feng, F.4
Wang, J.5
Wei, X.6
Yu, Z.7
Zhang, D.8
Zhang, Q.9
-
42
-
-
38049088818
-
Thiolated chitosan nanoparticles: Transfection study in the Caco-2 differentiated cell culture
-
Martien R, Loretz B, Sandbichler AM, Schnüch AB. (2008). Thiolated chitosan nanoparticles: transfection study in the Caco-2 differentiated cell culture. Nanotechnology, 19, 045101.
-
(2008)
Nanotechnology
, vol.19
, pp. 045101
-
-
Martien, R.1
Loretz, B.2
Sandbichler, A.M.3
Schnüch, A.B.4
-
43
-
-
61349095957
-
Development of an oral rutin nanocrystal formulation
-
Mauludin R, Müler RH, Keck CM. (2009). Development of an oral rutin nanocrystal formulation. Int J Pharm, 370, 202-209.
-
(2009)
Int. J. Pharm.
, vol.370
, pp. 202-209
-
-
Mauludin, R.1
Müler, R.H.2
Keck, C.M.3
-
45
-
-
21644468027
-
Insulin nanoparticles: A novel formulation approach for poorly water soluble Zn-insulin
-
Merisko-Liversidge E, McGurk SL, Liversidge GG. (2004). Insulin nanoparticles: a novel formulation approach for poorly water soluble Zn-insulin. Pharm Res, 21, 1545-1553.
-
(2004)
Pharm Res
, vol.21
, pp. 1545-1553
-
-
Merisko-Liversidge, E.1
McGurk, S.L.2
Liversidge, G.G.3
-
46
-
-
62749150964
-
Production and characterization of Hesperetin nanosuspensions for dermal delivery
-
Mishra PR, Al Shaal L, Müler RH, Keck CM. (2009). Production and characterization of Hesperetin nanosuspensions for dermal delivery. Int J Pharm, 371, 182-189.
-
(2009)
Int. J. Pharm.
, vol.371
, pp. 182-189
-
-
Mishra, P.R.1
Al Shaal, L.2
Müler, R.H.3
Keck, C.M.4
-
47
-
-
4644309307
-
Development of an intravenously injectable chemically stable aqueous omeprazole formulation using nanosuspension technology
-
Möchwitzer J, Achleitner G, Pomper H, Müler RH. (2004). Development of an intravenously injectable chemically stable aqueous omeprazole formulation using nanosuspension technology. Eur J Pharm Biopharm, 58, 615-619.
-
(2004)
Eur J Pharm Biopharm
, vol.58
, pp. 615-619
-
-
Möchwitzer, J.1
Achleitner, G.2
Pomper, H.3
Müler, R.H.4
-
48
-
-
79958005215
-
Potent dried drug nanosuspensions for oral bioavailability enhancement of poorly soluble drugs with pH-dependent solubility
-
Mou D, Chen H, Wan J, Xu H, Yang X. (2011). Potent dried drug nanosuspensions for oral bioavailability enhancement of poorly soluble drugs with pH-dependent solubility. Int J Pharm, 413, 237-244.
-
(2011)
Int. J. Pharm.
, vol.413
, pp. 237-244
-
-
Mou, D.1
Chen, H.2
Wan, J.3
Xu, H.4
Yang, X.5
-
49
-
-
0003649387
-
Zeta potential und Partikelladung-Kurze Theorie, praktische Meüdurchfuhrung
-
Medpharm Scientific, Stuttgart Stuttgart: Dateninterpretation, Wissenschaftliche
-
Muller RH. (1996). Zeta potential und Partikelladung-Kurze Theorie, praktische Meüdurchfuhrung. Stuttgart: Dateninterpretation, Wissenschaftliche
-
(1996)
Emulsions and nanosuspensions for the formulation of poorly soluble drugs
, pp. 149-173
-
-
Muller, R.H.1
Müler, R.H.2
Benita, S.3
Böm, B.4
-
51
-
-
0037177516
-
Buparvaquone mucoadhesive nanosuspension: Preparation, optimisation and long-term stability
-
Müler RH, Jacobs C. (2002). Buparvaquone mucoadhesive nanosuspension: preparation, optimisation and long-term stability. Int J Pharm, 237, 151-161.
-
(2002)
Int. J. Pharm.
, vol.237
, pp. 151-161
-
-
Müler, R.H.1
Jacobs, C.2
-
53
-
-
4544275025
-
Challenges and solutions for the delivery of biotech drugs-A review of drug nanocrystal technology and lipid nanoparticles
-
Muller RH, Keck CM. (2004). Challenges and solutions for the delivery of biotech drugs-a review of drug nanocrystal technology and lipid nanoparticles. J Biotechnol, 113, 151-170.
-
(2004)
J. Biotechnol
, vol.113
, pp. 151-170
-
-
Muller, R.H.1
Keck, C.M.2
-
54
-
-
28444461830
-
Drug nanocrystals of poorly soluble drugs produced by high pressure homogenization
-
Muller RH, Keck CM. (2006). Drug nanocrystals of poorly soluble drugs produced by high pressure homogenization. Eur J Pharm Biopharm, 62, 3-16.
-
(2006)
Eur J Pharm Biopharm
, vol.62
, pp. 3-16
-
-
Muller, R.H.1
Keck, C.M.2
-
55
-
-
0342897023
-
Nanosuspensions for the formulation of poorly soluble drugs-I. Preparation by a size-reduction technique
-
Muller RH, Peters K. (1998). Nanosuspensions for the formulation of poorly soluble drugs-I. Preparation by a size-reduction technique. Int J Pharm, 160, 229-237.
-
(1998)
Int. J. Pharm.
, vol.160
, pp. 229-237
-
-
Muller, R.H.1
Peters, K.2
-
56
-
-
0037400585
-
New micelle-like polymer aggregates made from PEI-PLGA diblock copolymers: Micellar characteristics and cellular uptake
-
Nam YS, Kang HS, Park JY, Park TG, Han SH, Chang IS. (2003). New micelle-like polymer aggregates made from PEI-PLGA diblock copolymers: micellar characteristics and cellular uptake. Biomaterials, 24, 2053-2059.
-
(2003)
Biomaterials
, vol.24
, pp. 2053-2059
-
-
Nam, Y.S.1
Kang, H.S.2
Park, J.Y.3
Park, T.G.4
Han, S.H.5
Chang, I.S.6
-
59
-
-
0031402134
-
Mucoadhesion of colloidal particulate systems in the gasrointesinal tract
-
Ponchel G, Montisci MJ, Dembri A. (1997). Mucoadhesion of colloidal particulate systems in the gasrointesinal tract. Eur J Pharm Biopharm, 4, 25-31
-
(1997)
Eur J Pharm Biopharm
, vol.4
, pp. 25-3
-
-
Ponchel, G.1
Montisci, M.J.2
Dembri, A.3
-
60
-
-
4544383493
-
Nanosuspensions in drug delivery
-
Rabinow BE. (2004). Nanosuspensions in drug delivery. Nat Rev Drug Discov, 3, 785-796.
-
(2004)
Nat Rev Drug Discov
, vol.3
, pp. 785-796
-
-
Rabinow, B.E.1
-
61
-
-
34250879747
-
Itraconazole IV nanosuspension enhances efficacy through altered pharmacokinetics in the rat
-
Rabinow B, Kipp J, Papadopoulos P, Wong J, Glosson J, Gass J, Sun CS, Wielgos T, White R, Cook C, Barker K, Wood K. (2007). Itraconazole IV nanosuspension enhances efficacy through altered pharmacokinetics in the rat. Int J Pharm, 339, 251-260.
-
(2007)
Int. J. Pharm.
, vol.339
, pp. 251-260
-
-
Rabinow, B.1
Kipp, J.2
Papadopoulos, P.3
Wong, J.4
Glosson, J.5
Gass, J.6
Sun, C.S.7
Wielgos, T.8
White, R.9
Cook, C.10
Barker, K.11
Wood, K.12
-
63
-
-
0032885450
-
Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs
-
Serajuddin AT. (1999). Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J Pharm Sci, 88, 1058-1066.
-
(1999)
J. Pharm Sci
, vol.88
, pp. 1058-1066
-
-
Serajuddin, A.T.1
-
64
-
-
79952999641
-
Development of nanosuspension formulation for oral delivery of quercetin
-
Sun M, Gao Y, Pei Y, Guo C, Li H, Cao F, Yu A, Zhai G. (2010). Development of nanosuspension formulation for oral delivery of quercetin. J Biomed Nanotechnol, 6, 325-332.
-
(2010)
J. Biomed Nanotechnol
, vol.6
, pp. 325-332
-
-
Sun, M.1
Gao, Y.2
Pei, Y.3
Guo, C.4
Li, H.5
Cao, F.6
Yu, A.7
Zhai, G.8
-
65
-
-
40949138845
-
Development of ascorbyl palmitate nanocrystals applying the nanosuspension technology
-
Teeranachaideekul V, Junyaprasert VB, Souto EB, Müler RH. (2008). Development of ascorbyl palmitate nanocrystals applying the nanosuspension technology. Int J Pharm, 354, 227-234.
-
(2008)
Int. J. Pharm.
, vol.354
, pp. 227-234
-
-
Teeranachaideekul, V.1
Junyaprasert, V.B.2
Souto, E.B.3
Müler, R.H.4
-
67
-
-
53949092998
-
Top-down production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products
-
Van den Mooter G, Van Eerdenbrugh B, Augustijns P. (2008a). Top-down production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products. Int J Pharm, 364, 64-75.
-
(2008)
Int. J. Pharm.
, vol.364
, pp. 64-75
-
-
Van Den Mooter, G.1
Van Eerdenbrugh, B.2
Augustijns, P.3
-
68
-
-
48849111481
-
Drying of crystalline drug nanosuspensions-The importance of surface hydrophobicity on dissolution behavior upon redispersion
-
Van den Mooter G, Van Eerdenbrugh B, Froyen L, Van Humbeeck J, Martens JA, Augustijns P. (2008b). Drying of crystalline drug nanosuspensions-The importance of surface hydrophobicity on dissolution behavior upon redispersion. Eur J Pharm Sci, 35, 127-135.
-
(2008)
Eur J Pharm Sci
, vol.35
, pp. 127-135
-
-
Van Den Mooter, G.1
Van Eerdenbrugh, B.2
Froyen, L.3
Van Humbeeck, J.4
Martens, J.A.5
Augustijns, P.6
-
69
-
-
69549119873
-
A comparative study of topdown and bottom-up approaches for the preparation of micro/ nanosuspensions
-
Verma S, Gokhale R, Burgess DJ. (2009a). A comparative study of topdown and bottom-up approaches for the preparation of micro/ nanosuspensions. Int J Pharm, 380, 216-222.
-
(2009)
Int. J. Pharm.
, vol.380
, pp. 216-222
-
-
Verma, S.1
Gokhale, R.2
Burgess, D.J.3
-
70
-
-
67649660193
-
Quality by design approach to understand the process of nanosuspension preparation
-
Verma S, Lan Y, Gokhale R, Burgess DJ. (2009b). Quality by design approach to understand the process of nanosuspension preparation. Int J Pharm, 377, 185-198.
-
(2009)
Int. J. Pharm.
, vol.377
, pp. 185-198
-
-
Verma, S.1
Lan, Y.2
Gokhale, R.3
Burgess, D.J.4
-
71
-
-
34547259640
-
Pharmacokinetic evaluation of a 1,3-dicyclohexylurea nanosuspension formulation to support early efficacy assessment
-
Wahlstrom JL, Chiang Po-Chang, Ghosh S, Warren CJ, Wene SP, A., Albin LA, Smith ME, Roberds SL. (2007). Pharmacokinetic evaluation of a 1,3-dicyclohexylurea nanosuspension formulation to support early efficacy assessment. Nanoscale Res Lett, 2, 291-296.
-
(2007)
Nanoscale Res Lett
, vol.2
, pp. 291-296
-
-
Wahlstrom, J.L.1
Po-Chang, C.2
Ghosh, S.3
Warren, C.J.4
Wene, S.P.A.5
Albin, L.A.6
Smith, M.E.7
Roberds, S.L.8
-
72
-
-
79957971638
-
Docetaxelloaded- lipid-based-nanosuspensions (DTX-LNS): Preparation, pharmacokinetics, tissue distribution and antitumor activity
-
Wang L, Liu Z, Liu D, Liu C, Juan Z, Zhang N. (2011a). Docetaxelloaded- lipid-based-nanosuspensions (DTX-LNS): preparation, pharmacokinetics, tissue distribution and antitumor activity. Int J Pharm, 413, 194-201.
-
(2011)
Int. J. Pharm.
, vol.413
, pp. 194-201
-
-
Wang, L.1
Liu, Z.2
Liu, D.3
Liu, C.4
Juan, Z.5
Zhang, N.6
-
73
-
-
78651430460
-
Development and in vitro evaluation of deacety mycoepoxydiene nanosuspension
-
Wang Y, Liu Z, Zhang D, Gao X, Zhang X, Duan C, Jia L, Feng F, Huang Y, Shen Y, Zhang Q. (2011b). Development and in vitro evaluation of deacety mycoepoxydiene nanosuspension. Colloids Surf B Biointerfaces, 83, 189-197.
-
(2011)
Colloids Surf B Biointerfaces
, vol.83
, pp. 189-197
-
-
Wang, Y.1
Liu, Z.2
Zhang, D.3
Gao, X.4
Zhang, X.5
Duan, C.6
Jia, L.7
Feng, F.8
Huang, Y.9
Shen, Y.10
Zhang, Q.11
-
74
-
-
77949885658
-
Vitro and in Vivo Evaluation of Silybin Nanosuspensions for Oral and Intravenous Delivery
-
Wang Y, Zhang D, Liu Z, Liu G, Duan C, Jia L, Feng F, Zhang X, Shi Y, Zhang Q. (2010). In vitro and in vivo evaluation of silybin nanosuspensions for oral and intravenous delivery. Nanotechnology, 21, 155104.
-
(2010)
Nanotechnology
, vol.21
, pp. 155104
-
-
Wang, Y.1
Zhang, D.2
Liu, Z.3
Liu, G.4
Duan, C.5
Jia, L.6
Feng, F.7
Zhang, X.8
Shi, Y.9
Zhang, Q.10
-
75
-
-
33751392855
-
Applications of microfluidics in chemical biology
-
Weibel DB, Whitesides GM. (2006). Applications of microfluidics in chemical biology. Curr Opin Chem Biol, 10, 584-591.
-
(2006)
Curr Opin Chem Biol
, vol.10
, pp. 584-591
-
-
Weibel, D.B.1
Whitesides, G.M.2
-
76
-
-
77953543307
-
Preparation of stable nitrendipine nanosuspensions using the precipitationultrasonication method for enhancement of dissolution and oral bioavailability
-
Xia D, Quan P, Piao H, Piao H, Sun S, Yin Y, Cui F. (2010). Preparation of stable nitrendipine nanosuspensions using the precipitationultrasonication method for enhancement of dissolution and oral bioavailability. Eur J Pharm Sci, 40, 325-334.
-
(2010)
Eur J Pharm Sci
, vol.40
, pp. 325-334
-
-
Xia, D.1
Quan, P.2
Piao, H.3
Piao, H.4
Sun, S.5
Yin, Y.6
Cui, F.7
-
77
-
-
38349162256
-
Preparation and characterization of intravenously injectable nimodipine nanosuspension
-
Xiong R, Lu W, Li J, Wang P, Xu R, Chen T. (2008). Preparation and characterization of intravenously injectable nimodipine nanosuspension. Int J Pharm, 350, 338-343.
-
(2008)
Int. J. Pharm.
, vol.350
, pp. 338-343
-
-
Xiong, R.1
Lu, W.2
Li, J.3
Wang, P.4
Xu, R.5
Chen, T.6
-
78
-
-
77951652999
-
Comparison of bioavailability of amorphous versus crystalline itraconazole nanoparticles via pulmonary administration in rats
-
Yang W, Johnston KP, Williams RO 3rd. (2010). Comparison of bioavailability of amorphous versus crystalline itraconazole nanoparticles via pulmonary administration in rats. Eur J Pharm Biopharm, 75, 33-41.
-
(2010)
Eur J Pharm Biopharm
, vol.75
, pp. 33-41
-
-
Yang, W.1
Johnston, K.P.2
Williams III, R.O.3
-
79
-
-
77952741121
-
Preparation and cytotoxic activity of hydroxycamptothecin nanosuspensions
-
Zhao YX, Hua HY, Chang M, Liu WJ, Zhao Y, Liu HM. (2010). Preparation and cytotoxic activity of hydroxycamptothecin nanosuspensions. Int J Pharm, 392, 64-71.
-
(2010)
Int. J. Pharm.
, vol.392
, pp. 64-71
-
-
Zhao, Y.X.1
Hua, H.Y.2
Chang, M.3
Liu, W.J.4
Zhao, Y.5
Liu, H.M.6
-
80
-
-
79957635086
-
Vitro antitumor activity of silybin nanosuspension in PC-3 cells
-
Zheng D, Wang Y, Zhang D, Liu Z, Duan C, Jia L, Wang F, Liu Y, Liu G, Hao L, Zhang Q. (2011). In vitro antitumor activity of silybin nanosuspension in PC-3 cells. Cancer Lett, 307, 158-164.
-
(2011)
Cancer Lett
, vol.307
, pp. 158-164
-
-
Zheng, D.1
Wang, Y.2
Zhang, D.3
Liu, Z.4
Duan, C.5
Jia, L.6
Wang, F.7
Liu, Y.8
Liu, G.9
Hao, L.10
Zhang, Q.11
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