000			02127pam a2200421 i 4500
999			_c10502 _d10502
001			4378979
005			20210307110347.0
008			910712s1992 nyua b 001 0 eng c
010			_a 91025103
020			_a9780824785673
020			_a0824785673 (alk. paper)
040			_aDNLM/DLC _cDLC _dDLC _erda
050	0	0	_aRS189 _b.B28 1991
060			_aW1 DR893B v. 49 _aQV 38 B212p
082	0	0	_a615.19 _222 _bB.U.P
100	1		_aBanakar, Umesh V., _d1956-, _eauthor.
245	1	0	_aPharmaceutical dissolution testing / _cUmesh V. Banakar ; with contributions by William A Hanson ... [et al.].
264		1	_aNew York : _bMarcel Dekker Inc., _c[1992]
264		4	_c©1992
300			_aix, 437 pages : _billustrations ; _c24 cm
336			_2rdacontent _atext
337			_2rdamedia _aunmediated
338			_2rdacarrier _avolume
490	1		_aDrugs and the pharmaceutical sciences ; _vv. 49
500			_apharmacy bookfair2016
504			_aIncludes bibliographical references and indexes.
505	0		_a"Introduction, Historical Highlights, and the Need for Dissolution Testing Theories of Dissolution Dissolution Testing Devices Automation in Dissolution Testing, by William A. Hanson and Albertha M. Paul Factors That Influence Dissolution Testing Interpretation of Dissolution Rate Data Techniques and of In Vivo Dissolution, by Umesh V. Banakar, Chetan D. Lathia, and John H. Wood Dissolution of Dosage Forms Dissolution of Modified-Release Dosage Forms Dissolution and Bioavailability Dissolution Testing and the Assessment of Bioavailability/Bioequivalence, by Santosh J. Vetticaden Dissolution Rediscovered, by John H. Wood Appendix: USP/NF Dissolution Test "
650		0	_aDrugs _xSolubility _xTesting.
650		2	_aBiological Availability.
650		2	_aSolubility.
650		2	_aTechnology, Pharmaceutical _xmethods.
830		0	_tDrugs and the pharmaceutical sciences
856			_3Abstract _uhttp://repository.fue.edu.eg/xmlui/handle/123456789/1823
906			_a7 _bcbc _corignew _d1 _eocip _f19 _gy-gencatlg
942			_2ddc _cBK