Alfuzosin Hydrochloride Transdermal Films: Evaluation of Physicochemical, In Vitro Human Cadaver Skin Permeation and Thermodynamic Parameters

被引:13
作者
Pattnaik, Satyanarayan [1 ]
Swain, Kalpana
Choudhury, Parthagan
Acharya, Pradeepta K.
Mallick, Subrata [2 ]
机构
[1] Coll Pharmaceut Sci, Dept Pharmaceut, Percutaneous Drug Delivery Syst, Berhampur 760002, Orissa, India
[2] SOA Univ, Sch Pharmaceut Sci, Bhubaneswar, Orissa, India
来源
INTERNATIONAL BRAZ J UROL | 2009年 / 35卷 / 06期
关键词
alfuzosin hydrochloride; administration; cutaneous; polymers; DRUG-RELEASE; DELIVERY; DESIGN; EFFICACY; SYSTEM;
D O I
10.1590/S1677-55382009000600010
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: The main objective of the investigation was to develop a transdermal therapeutic system for alfuzosin hydrochloride and to study the effects of polymeric system and loading dose on the in vitro skin permeation pattern. Materials and Methods: Principles of experimental design have been exploited to develop the dosage form. Ratio of ethyl cellulose (EC) and polyvinyl pyrrolidone (PVP) and loading dose were selected as independent variables and their influence on the cumulative amount of alfuzosin hydrochloride permeated per cm(2) of human cadaver skin at 24 h (Q(24)), permeation flux (J) and steady state permeability coefficient (P-ss) were studied using experimental design. Various physicochemical parameters of the transdermal films were also evaluated. Activation energy for in vitro transdermal permeation has been estimated. Results: Ratio of EC and PVP was found to be the main influential factor for all the dependent variables studied. Drug loading dose was also found to influence the dependent variables but to a lesser extent. Physicochemical parameters of the prepared films were evaluated and found satisfactory. Activation energy for alfuzosin permeation has also been estimated and reported. Conclusion: The therapeutic system was found to be dermatologically non-irritant and hence, a therapeutically effective amount of alfuzosin hydrochloride can be delivered via a transdermal route.
引用
收藏
页码:716 / 729
页数:14
相关论文
共 20 条
[1]   Design, development, physicochemical, and in vitro and in vivo evaluation of transdermal patches containing diclofenac diethylammonium salt [J].
Arora, P ;
Mukherjee, B .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (09) :2076-2089
[2]  
Barat Romi, 2007, Acta Pharmaceutica (Zagreb), V57, P469, DOI 10.2478/v10007-007-0037-1
[3]   Breaching the skin's barrier to drugs [J].
Barry, BW .
NATURE BIOTECHNOLOGY, 2004, 22 (02) :165-167
[4]   EFFECT OF VARYING DRUG LOADING ON PARTICLE-SIZE DISTRIBUTION AND DRUG-RELEASE KINETICS OF VERAPAMIL HYDROCHLORIDE MICROSPHERES PREPARED WITH CELLULOSE ESTERS [J].
BHARDWAJ, SB ;
SHUKLA, AJ ;
COLLINS, CC .
JOURNAL OF MICROENCAPSULATION, 1995, 12 (01) :71-81
[5]   EVALUATION OF DRUG-CONTAINING POLYMER-FILMS PREPARED FROM AQUEOUS LATEXES [J].
BODMEIER, R ;
PAERATAKUL, O .
PHARMACEUTICAL RESEARCH, 1989, 6 (08) :725-730
[6]   A meta-analysis on the efficacy and tolerability of α1-adrenoceptor antagonists in patients with lower urinary tract symptoms suggestive of benign prostatic obstruction [J].
Djavan, B ;
Marberger, M .
EUROPEAN UROLOGY, 1999, 36 (01) :1-12
[7]  
Draize JH, 1944, J PHARMACOL EXP THER, V82, P377
[8]   HIGH PREVALENCE OF BENIGN PROSTATIC HYPERTROPHY IN THE COMMUNITY [J].
GARRAWAY, WM ;
COLLINS, GN ;
LEE, RJ .
LANCET, 1991, 338 (8765) :469-471
[9]   MECHANISMS OF CORNEAL DRUG PENETRATION .1. INVIVO AND INVITRO KINETICS [J].
GRASS, GM ;
ROBINSON, JR .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1988, 77 (01) :3-14
[10]   Design and in vitro evaluation of adhesive matrix for transdermal delivery of propranolol [J].
Guyot, M ;
Fawaz, F .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 204 (1-2) :171-182