In vitro permeation screening of a new formulation of thiocolchicoside containing various enhancers

被引:7
作者
Ceschel, GC
Maffei, P
Porzio, S
Melillo, G
Caselli, GF
Dragani, MC
Gentile, MM
Clavenna, G
机构
[1] Univ Bologna, Dept Pharmaceut Sci, I-40128 Bologna, Italy
[2] Dompe SpA, Laquila, Italy
关键词
DPPG; enhancer; percutaneous absorption; thiocolchicoside;
D O I
10.1080/10717540260397882
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Thiocolchicoside, a muscle relaxant agent with anti-inflammatory and analgesic actions, also is used topically for the treatment of muscular spasms and for rheumatologic, orthopedic, and traumatologic disorders. In this study, thiocolchicoside was formulated to use as foam to avoid contact with the afflicted area during the spreading phase. To enhance drug penetration, various enhancers were added to the base formulation. The tested enhancers were ethoxyethylendiglycol (Transcutol(R)), highly purified phosphatidylcholine (Lipoid S20), capsaicin, propylene glycol dipelargonate (DPPG), and glycolysed ethoxylated glycerides (Labrafil M1944 CS). The transdermal absorption of the tested formulations containing enhancers, in comparison with base formulation, was evaluated in vitro through rat skin using standard Franz diffusion cells. Base formulation was found to have a higher permeation profile than the simple aqueous and hydroalcoholic solutions of the drug, meaning that the base formulation by itself enhances the drug permeation. Among the tested formulations, only the formulation containing DPPG/ethanol was found to be statistically different, showing an enhancement factor of 3.58. In the same experimental session, Muscoril(R) ointment, the commercially available pharmaceutical product containing the same thiocolchicoside concentration (0.25%), also was tested. The formulation containing DPPG/ ethanol showed a 4.86 times increase of permeability constant in comparison with Muscoril(R) ointment. The formulation containing DPPG/ ethanol as an enhancer could be a good candidate for a new topical foam, considering its good characteristics of permeability and compliance.
引用
收藏
页码:259 / 263
页数:5
相关论文
共 23 条
[1]   PIROXICAM RELEASE FROM DERMATOLOGICAL BASES - INVITRO STUDIES USING CELLULOSE MEMBRANE AND HAIRLESS MOUSE SKIN [J].
BABAR, A ;
SOLANKI, UD ;
CUTIE, AJ ;
PLAKOGIANNIS, F .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1990, 16 (03) :523-540
[2]   TRANSDERMAL PERMEATION OF VASOPRESSIN .2. INFLUENCE OF AZONE ON INVITRO AND INVIVO PERMEATION [J].
BANERJEE, PS ;
RITSCHEL, WA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 49 (03) :199-204
[3]  
BARRY B W, 1987, Journal of Controlled Release, V6, P85, DOI 10.1016/0168-3659(87)90066-6
[4]   EFFECTS OF SOME NONTOXIC PENETRATION ENHANCERS ON IN-VITRO HEPARIN SKIN PERMEATION FROM GEL VEHICLES [J].
BONINA, FP ;
MONTENEGRO, L .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 111 (02) :191-196
[5]   VEHICLE EFFECTS ON IN-VITRO SKIN PERMEATION OF AND STRATUM-CORNEUM AFFINITY FOR MODEL-DRUGS CAFFEINE AND TESTOSTERONE [J].
BONINA, FP ;
CARELLI, V ;
DICOLO, G ;
MONTENEGRO, L ;
NANNIPIERI, E .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 100 (1-3) :41-47
[6]   The effects of Azone and capsaicin on the permeation of naproxen through human skin [J].
Degim, IT ;
Uslu, A ;
Hadgraft, J ;
Atay, T ;
Akay, C ;
Cevheroglu, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 179 (01) :21-25
[7]   Capsaicin and nonivamide as novel skin permeation enhancers for indomethacin [J].
Fang, JY ;
Fang, CL ;
Hong, CT ;
Chen, HY ;
Lin, TY ;
Wei, HM .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 12 (03) :195-203
[8]   MASS-TRANSPORT PHENOMENA AND MODELS - THEORETICAL CONCEPTS [J].
FLYNN, GL ;
YALKOWSKY, SH ;
ROSEMAN, TJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1974, 63 (04) :479-510
[9]   PERCUTANEOUS ABSORPTION - RELEVANCE OF INVITRO DATA [J].
FRANZ, TJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1975, 64 (03) :190-195
[10]   KINETICS OF CUTANEOUS DRUG PENETRATION [J].
FRANZ, TJ .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1983, 22 (09) :499-505