Gao P - Search Results

1

Mechanistic analysis of solute transport in an in vitro physiological two-phase dissolution apparatus.

Mudie DM, Shi Y, Ping H, Gao P, Amidon GL, Amidon GE. Mudie DM, et al. Among authors: gao p. Biopharm Drug Dispos. 2012 Oct;33(7):378-402. doi: 10.1002/bdd.1803. Epub 2012 Sep 4. Biopharm Drug Dispos. 2012. PMID: 22847296 Free PMC article.

2

In Vivo Predictive Dissolution and Simulation Workshop Report: Facilitating the Development of Oral Drug Formulation and the Prediction of Oral Bioperformance.

Tsume Y, Patel S, Fotaki N, Bergstrӧm C, Amidon GL, Brasseur JG, Mudie DM, Sun D, Bermejo M, Gao P, Zhu W, Sperry DC, Vertzoni M, Parrott N, Lionberger R, Kambayashi A, Hermans A, Lu X, Amidon GE. Tsume Y, et al. Among authors: gao p. AAPS J. 2018 Sep 6;20(6):100. doi: 10.1208/s12248-018-0260-3. AAPS J. 2018. PMID: 30191341 Free PMC article. No abstract available.

3

Application of a biphasic test for characterization of in vitro drug release of immediate release formulations of celecoxib and its relevance to in vivo absorption.

Shi Y, Gao P, Gong Y, Ping H. Shi Y, et al. Among authors: gao p. Mol Pharm. 2010 Oct 4;7(5):1458-65. doi: 10.1021/mp100114a. Epub 2010 Aug 12. Mol Pharm. 2010. PMID: 20704265

4

Characterization of supersaturatable formulations for improved absorption of poorly soluble drugs.

Gao P, Shi Y. Gao P, et al. AAPS J. 2012 Dec;14(4):703-13. doi: 10.1208/s12248-012-9389-7. Epub 2012 Jul 14. AAPS J. 2012. PMID: 22798021 Free PMC article. Review.

5

Assessing Supersaturation and Its Impact on In Vivo Bioavailability of a Low-Solubility Compound ABT-072 With a Dual pH, Two-Phase Dissolution Method.

Shi Y, Erickson B, Jayasankar A, Lu L, Marsh K, Menon R, Gao P. Shi Y, et al. Among authors: gao p. J Pharm Sci. 2016 Sep;105(9):2886-2895. doi: 10.1016/j.xphs.2016.04.036. Epub 2016 Jun 16. J Pharm Sci. 2016. PMID: 27321234 Clinical Trial.

6

In vitro characterization of ritonavir formulations and correlation to in vivo performance in dogs.

Xu H, Krakow S, Shi Y, Rosenberg J, Gao P. Xu H, et al. Among authors: gao p. Eur J Pharm Sci. 2018 Mar 30;115:286-295. doi: 10.1016/j.ejps.2018.01.026. Eur J Pharm Sci. 2018. PMID: 29355594

7

Developing Quantitative In Vitro-In Vivo Correlation for Fenofibrate Immediate-Release Formulations With the Biphasic Dissolution-Partition Test Method.

Xu H, Shi Y, Vela S, Marroum P, Gao P. Xu H, et al. Among authors: gao p. J Pharm Sci. 2018 Jan;107(1):476-487. doi: 10.1016/j.xphs.2017.06.018. Epub 2017 Jun 27. J Pharm Sci. 2018. PMID: 28666964 Clinical Trial.

8

In Vitro Characterization of Ritonavir Drug Products and Correlation to Human in Vivo Performance.

Xu H, Vela S, Shi Y, Marroum P, Gao P. Xu H, et al. Among authors: gao p. Mol Pharm. 2017 Nov 6;14(11):3801-3814. doi: 10.1021/acs.molpharmaceut.7b00552. Epub 2017 Sep 27. Mol Pharm. 2017. PMID: 28898584

9

Characterization of the Partition Rate of Ibuprofen Across the Water-Octanol Interface and the Influence of Common Pharmaceutical Excipients.

Xu H, Wang W, Shi Y, Gao P. Xu H, et al. Among authors: gao p. J Pharm Sci. 2019 Jan;108(1):525-537. doi: 10.1016/j.xphs.2018.11.026. Epub 2018 Nov 22. J Pharm Sci. 2019. PMID: 30471290

10

Development of supersaturatable self-emulsifying drug delivery system formulations for improving the oral absorption of poorly soluble drugs.

Gao P, Morozowich W. Gao P, et al. Expert Opin Drug Deliv. 2006 Jan;3(1):97-110. doi: 10.1517/17425247.3.1.97. Expert Opin Drug Deliv. 2006. PMID: 16370943 Review.

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