Enhanced rectal absorption of insulin-loaded Pluronic® F-127 gels containing unsaturated fatty acids

被引:45
作者
Barichello, JM
Morishita, M
Takayama, K
Chiba, Y
Tokiwa, S
Nagai, T
机构
[1] Hoshi Univ, Fac Pharmaceut Sci, Dept Pharmaceut, Shinagawa Ku, Tokyo 1428501, Japan
[2] Nippon Suisan Kaisya, Cent Res Lab, Hachioji, Tokyo 1920906, Japan
关键词
insulin; Pluronic F-127 gels; rectal absorption; unsaturated fatty acids; hypoglycermic effect; sustained release;
D O I
10.1016/S0378-5173(99)00090-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The objective of this study was to prepare and to evaluate Pluronic F-127 (PF127) gel containing unsaturated fatty acids such as oleic acid (18:1), eicosapentaenoic acid (20:5) and docosahexaenoic acid (22:6) as a potential formulation for rectal delivery of insulin. The hypoglycemic effect of insulin was examined following rectal administration of the various formulations in normal rats. Rectal insulin absorption was markedly enhanced, and marked hypoglycemia was induced by all PF127 gels (insulin dose, 5 U/kg) containing different unsaturated fatty acids. PF127 gels containing unsaturated fatty acids presented low t(max) mean values indicating that the absorption of insulin occurred very rapidly in the rectum. The relative hypoglycemic efficacy of PF127 gel formulations containing fatty acids such as oleic acid, eicosapentaenoic (EPA) and docosahexaenoic (DHA) were 28.4 +/- 8.1, 26.8 +/- 14.3 and 23.1 +/- 5.7%, respectively. The finding demonstrated that 20% PF127 gels containing unsaturated fatty acids are potential formulations for rectal delivery of insulin. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:125 / 132
页数:8
相关论文
共 41 条
[1]  
BARICHELLO JM, 1998, UNPUB INT J PHARM
[2]   LYMPHATIC UPTAKE OF WATER-SOLUBLE DRUGS AFTER RECTAL ADMINISTRATION [J].
CALDWELL, L ;
NISHIHATA, T ;
RYTTING, JH ;
HIGUCHI, T .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1982, 34 (08) :520-522
[3]  
CHENCHOW PC, 1981, INT J PHARM, V8, P89
[4]   Development of in situ gelling and mucoadhesive acetaminophen liquid suppository [J].
Choi, HG ;
Jung, JH ;
Ryu, JM ;
Yoon, SJ ;
Oh, YK ;
Kim, CK .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 165 (01) :33-44
[5]   In situ gelling and mucoadhesive liquid suppository containing acetaminophen: enhanced bioavailability [J].
Choi, HG ;
Oh, YK ;
Kim, CK .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 165 (01) :23-32
[6]   In vitro evaluation of pluronic F127-based controlled-release ocular delivery systems for pilocarpine [J].
Desai, SD ;
Blanchard, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (02) :226-230
[7]   Rheological evaluation of poloxamer as an in situ gel for ophthalmic use [J].
Edsman, K ;
Carlfors, J ;
Petersson, R .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 6 (02) :105-112
[8]   MULTIPLE SEQUENCE ELEMENTS IN THE C-FOS PROMOTER MEDIATE INDUCTION BY CAMP [J].
FISCH, TM ;
PRYWES, R ;
SIMON, MC ;
ROEDER, RG .
GENES & DEVELOPMENT, 1989, 3 (02) :198-211
[9]   AN ELECTRON-SPIN RESONANCE STUDY OF SKIN PENETRATION ENHANCERS [J].
GAY, CL ;
MURPHY, TM ;
HADGRAFT, J ;
KELLAWAY, IW ;
EVANS, JC ;
ROWLANDS, CC .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 49 (01) :39-45
[10]   Pharmacokinetic considerations of new insulin formulations and routes of administration [J].
Hoffman, A ;
Ziv, E .
CLINICAL PHARMACOKINETICS, 1997, 33 (04) :285-301