MARC보기
LDR02052nmm uu200409 4500
001000000332159
00520240805170141
008181129s2018 |||||||||||||||||c||eng d
020 ▼a 9780438239340
035 ▼a (MiAaPQ)AAI10954445
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 615
1001 ▼a Setiawan, Nico.
24510 ▼a Understanding the Thermodynamics and Oral Absorption Potential of Pharmaceutical Amorphous Solid Dispersions.
260 ▼a [S.l.] : ▼b University of Kentucky., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 159 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 ▼a Adviser: Patrick J. Marsac.
5021 ▼a Thesis (Ph.D.)--University of Kentucky, 2018.
520 ▼a Supersaturating drug delivery systems, such as amorphous solid dispersions (ASDs), have been used extensively to elevate the apparent solubility and oral bioavailability of poorly water-soluble drugs. However, despite the numerous examples of su
520 ▼a Further, ASDs must dissolve after administration and maintain the intended supersaturation in the gastrointestinal (GI) tract during the GI transit time to achieve maximum oral absorption. In solution, the energetics advantage of the amorphous o
520 ▼a 1. The relative thermodynamics magnitude of various processes with respect to the crystallization energy associated with amorphous drugs 2. The development of a practical tool to measure the thermodynamic activity of amorphous materials over its
590 ▼a School code: 0102.
650 4 ▼a Pharmaceutical sciences.
650 4 ▼a Chemical engineering.
690 ▼a 0572
690 ▼a 0542
71020 ▼a University of Kentucky. ▼b Pharmacy.
7730 ▼t Dissertation Abstracts International ▼g 79-12B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0102
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T15001224 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자