Improving the dissolution and oral bioavailability of the poorly water-soluble drug aloe-emodin by solid dispersion with polyethylene glycol 6000
Hao-gang Duan; Yu-hui Wei; Bo-xia Li; Hong-yan Qin; Xin-an Wu
Drug Development Research 70(5): 363-369
2009
ISSN/ISBN: 0272-4391
DOI: 10.1002/ddr.20312
Accession: 063802700
PDF emailed within 0-6 h: $19.90
Related References
Joshi, H.N.; Tejwani, R.W.; Davidovich, M.; Sahasrabudhe, V.P.; Jemal, M.; Bathala, M.S.; Varia, S.A.; Serajuddin, A.T.M. 2004: Bioavailability enhancement of a poorly water-soluble drug by solid dispersion in polyethylene glycol-polysorbate 80 mixture International Journal of Pharmaceutics 269(1): 251-258Serajuddin, A.T.; Sheen, P.C.; Augustine, M.A. 1990: Improved dissolution of a poorly water-soluble drug from solid dispersions in polyethylene glycol: polysorbate 80 mixtures Journal of Pharmaceutical Sciences 79(5): 463-464
Chokshi, R.J.; Zia, H.; Sandhu, H.K.; Shah, N.H.; Malick, W.A. 2007: Improving the dissolution rate of poorly water soluble drug by solid dispersion and solid solution: pros and cons Drug Delivery 14(1): 33-45
Rivera, W.; Ghaly, E.S.; Marti, A. 1991: Comparative evaluation of polyethylene glycol 4000 and poloxamer as solid dispersion systems for a poorly water soluble antidiabetic drug Pharmaceutical Research (New York) 8(10 Suppl): S89
Dannenfelser, R.-M.; He, H.; Joshi, Y.; Bateman, S.; Serajuddin, A.T.M. 2004: Development of clinical dosage forms for a poorly water soluble drug I: Application of polyethylene glycol-polysorbate 80 solid dispersion carrier system Journal of Pharmaceutical Sciences 93(5): 1165-1175
Tran, P.; Park, J-Sook. 2021: Formulation of solid dispersion to improve dissolution and oral bioavailability of poorly soluble dexibuprofen Pharmaceutical Development and Technology 2021: 1-33
Guo, S.; Pham, K.; Li, D.; Penzak, S.R.; Dong, X. 2016: Novel in situ self-assembly nanoparticles for formulating a poorly water-soluble drug in oral solid granules, improving stability, palatability, and bioavailability International Journal of Nanomedicine 11: 1451-1460
My Tran, K.Thi.; Vo, T.Van.; Lee, B-Jin.; Duan, W.; Ha-Lien Tran, P.; Truong-Dinh Tran, T. 2018: Encapsulation of Solid Dispersion in Solid Lipid Particles for Dissolution Enhancement of Poorly Water-Soluble Drug Current Drug Delivery 15(4): 576-584
Sheen, P.C.; Kim, S.I.; Petillo, J.J.; Serajuddin, A.T. 1991: Bioavailability of a poorly water-soluble drug from tablet and solid dispersion in humans Journal of Pharmaceutical Sciences 80(7): 712-714
Serajuddin, A.T.; Sheen, P.C.; Mufson, D.; Bernstein, D.F.; Augustine, M.A. 1988: Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersions Journal of Pharmaceutical Sciences 77(5): 414-417
Sinha, S.; Ali, M.; Baboota, S.; Ahuja, A.; Kumar, A.; Ali, J. 2010: Solid dispersion as an approach for bioavailability enhancement of poorly water-soluble drug ritonavir Aaps Pharmscitech 11(2): 518-527
Yano, K.; Kajiyama, A.; Itoh, N.; Shimaya, J.; Yamamoto, K. 1997: Improvement of bioavailability of poorly water-soluble drug by nanoparticles from a solid dispersion system Yakuzaigaku 57(2): 95-101
Wan, S.; Sun, Y.; Qi, X.; Tan, F. 2012: Improved bioavailability of poorly water-soluble drug curcumin in cellulose acetate solid dispersion Aaps Pharmscitech 13(1): 159-166
Zakeri-Milani, P.; Hallaj Nezhadi, S.; Barzegar-Jalali, M.; Mohammadi, L.; Nokhodchi, A.; Valizadeh, H. 2011: Studies on dissolution enhancement of prednisolone, a poorly water-soluble drug by solid dispersion technique Advanced Pharmaceutical Bulletin 1(1): 48-53
Liu, C.; Liu, Z.; Chen, Y.; Chen, Z.; Chen, H.; Pui, Y.; Qian, F. 2018: Oral bioavailability enhancement of β-lapachone, a poorly soluble fast crystallizer, by cocrystal, amorphous solid dispersion, and crystalline solid dispersion European Journal of Pharmaceutics and Biopharmaceutics: Official Journal of Arbeitsgemeinschaft für Pharmazeutische Verfahrenstechnik E.V 124: 73-81
Tran, T.T.-D.; Tran, P.H.-L.; Lee, B.-J. 2009: Dissolution-modulating mechanism of alkalizers and polymers in a nanoemulsifying solid dispersion containing ionizable and poorly water-soluble drug European Journal of Pharmaceutics and Biopharmaceutics: Official Journal of Arbeitsgemeinschaft für Pharmazeutische Verfahrenstechnik E.V 72(1): 83-90
Ohara, T.; Kitamura, S.; Kitagawa, T.; Terada, K. 2005: Dissolution mechanism of poorly water-soluble drug from extended release solid dispersion system with ethylcellulose and hydroxypropylmethylcellulose International Journal of Pharmaceutics 302(1-2): 95-102
Zhang, Y.; Che, E.; Zhang, M.; Sun, B.; Gao, J.; Han, J.; Song, Y. 2014: Increasing the dissolution rate and oral bioavailability of the poorly water-soluble drug valsartan using novel hierarchical porous carbon monoliths International Journal of Pharmaceutics 473(1-2): 375-383
Murali Mohan Babu, G.V.; Kumar, N.R.; Sankar, K.H.; Ram, B.J.; Kumar, N.K.; Murthy, K.V.R. 2002: In vivo evaluation of modified gum karaya as a carrier for improving the oral bioavailability of a poorly water-soluble drug, nimodipine Aaps Pharmscitech 3(2): E12
Chiba, Y.; Kohri, N.; Iseki, K.; Miyazaki, K. 1991: Improvement of dissolution and bioavailability for mebendazole, an agent for human echinococcosis, by preparing solid dispersion with polyethylene glycol Chemical and Pharmaceutical Bulletin 39(8): 2158-2160