Simulated Biological Fluids with Possible Application in Dissolution Testing

被引:859
作者
Marques, Margareth R. C. [1 ]
Loebenberg, Raimar [2 ]
Almukainzi, May [2 ]
机构
[1] US Pharmacopeia, Rockville, MD 20852 USA
[2] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB T6J 2L7, Canada
来源
DISSOLUTION TECHNOLOGIES | 2011年 / 18卷 / 03期
关键词
HUMAN GASTROINTESTINAL-TRACT; IN-VIVO DISSOLUTION; CORROSION BEHAVIOR; APATITE FORMATION; ARTIFICIAL SWEAT; MAGNESIUM ALLOYS; DELIVERY-SYSTEM; DISSOLVING FILM; SILICA-GEL; VITRO;
D O I
10.14227/DT180311P15
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
This literature review is a compilation of the composition and, in most cases, the preparation instructions for simulated biological fluids that may be used as dissolution media in the evaluation of dissolution profiles and amount of drug released from pharmaceutical dosage forms. The use of simulated biological fluids can give a better understanding of the release mechanisms and possible in vivo behavior of a product and enhance the predictive capability of the dissolution testing. A summary of the major characteristics of the most used routes of administration that may affect dissolution and absorption of drug substances is presented. The routes and simulated biological fluids covered by this review are: Parenteral: simulated body fluid and simulated synovial fluid. Oral: fasted-state simulated gastric fluid, fed-state simulated gastric fluid, fasted-state simulated intestinal fluid, fed-state simulated intestinal fluid, simulated colonic fluid, fasted-state simulated colonic fluid, and fed-state simulated colonic fluid. Buccal and sublingual: simulated saliva. Pulmonary: simulated lung fluid. Vaginal: simulated vaginal fluid and simulated semen. Ophthalmic: simulated tears. Simulated sweat is also included. Some examples of how these simulated biological fluids are used to evaluate dosage forms are included in each route of administration.
引用
收藏
页码:15 / 28
页数:14
相关论文
共 58 条
[1]
Release of dithiocarbamates into artificial sweat from latex vulcanizates: Effects of the accelerator type and storage time [J].
Abraham, Elizabeth K. ;
Ramesh, P. ;
Joseph, R. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2006, 102 (03) :2055-2061
[2]
Abraham Sindhu, 2007, Indian Journal of Pharmaceutical Sciences, V69, P24
[3]
Polymer-lipid based mucoadhesive microspheres prepared by spray-congealing for the vaginal delivery of econazole nitrate [J].
Albertini, Beatrice ;
Passerini, Nadia ;
Di Sabatino, Marcello ;
Vitali, Beatrice ;
Brigidi, Patrizia ;
Rodriguez, Lorenzo .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 36 (4-5) :591-601
[4]
Design and evaluation of novel fast forming pilocarpine-loaded ocular hydrogels for sustained pharmacological response [J].
Anumolu, SivaNaga S. ;
Singh, Yashveer ;
Gao, Dayuan ;
Stein, Stanley ;
Sinko, Patrick J. .
JOURNAL OF CONTROLLED RELEASE, 2009, 137 (02) :152-159
[5]
Aswar P., 2009, Arch. Pharm. Sci. Res, V1, P48
[6]
Current perspectives in dissolution testing of conventional and novel dosage forms [J].
Azarmi, Shirzad ;
Roa, Wilson ;
Lobenberg, Raimar .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 328 (01) :12-21
[7]
Instant FaSSIF and FeSSIF-Biorelevance Meets Practicality [J].
Boni, Julia Elisabeth ;
Brickl, Rolf Stefan ;
Dressman, Jennifer ;
Pfefferle, Martin L. .
DISSOLUTION TECHNOLOGIES, 2009, 16 (03) :41-45
[8]
*BRIT STAND I, 1999, 1811 BS EN BRIT STAN
[9]
Chang C, 2007, J BIOMAT SCI-POLYM E, V18, P1591
[10]
Resistant starch as a carrier for oral colon-targeting drug matrix system [J].
Chen, Ling ;
Li, Xiaoxi ;
Pang, Yansheng ;
Li, Lin ;
Zhang, Ximei ;
Yu, Long .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2007, 18 (11) :2199-2203