Oil-in-water lipid emulsions: implications for parenteral and ocular delivering systems

被引:119
作者
Tamilvanan, S [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Dept Pharmaceut, Sector 67, Nagar 160062, Punjab, India
关键词
emulsion; parenteral; plasma proteins; ocular;
D O I
10.1016/j.plipres.2004.09.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid emulsions (LEs) are heterogenous dispersions of two immiscible liquids (oil-in-water or water-in-oil) and they are subjected to various instability processes like aggregation, flocculation, coalescence and hence eventual phase separation according to the second law of thermodynamics. However, the physical stability of the LE can substantially be improved with help of suitable emulsifiers that are capable of forming a mono- or multi-layer coating film around the dispersed liquid droplets in such a way to reduce interfacial tension or to increase droplet-droplet repulsion. Depending on the concentrations of these three components (oil-water-emulsifier) and the efficiency of the emulsification equipments used to reduce droplet size, the final LE may be in the form of oil-in-water (o/w), water-in-oil (w/o), micron, submicron and double or multiple emulsions (o/w/o and w/o/w). The o/w type LEs (LE) are colloidal drug carriers, which have various therapeutic applications. As an intravenous delivery system it incorporates lipophilic water non-soluble drugs, stabilize drugs that tend to undergo hydrolysis and reduce side effects of various potent drugs. When the LE is used as an ocular delivery systems they increase local bioavailability, sustain the pharmacological effect of drugs and decrease systemic side effects of the drugs. Thus, the rationale of using LE as an integral part of effective treatment is clear. Following administration of LE through these routes, the biofate of LE associated bioactive molecules are somehow related to the vehicles disposition kinetics inside blood or eyeball. However, the LE is not devoid from undergoing various bio-process while exerting their efficacious actions. The purpose of this review is therefore to give an implication of LE for parenteral and ocular delivering systems. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:489 / 533
页数:45
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共 248 条
[71]  
GOLDBERG IJ, 1990, J BIOL CHEM, V265, P4266
[72]   BIODEGRADABLE LONG-CIRCULATING POLYMERIC NANOSPHERES [J].
GREF, R ;
MINAMITAKE, Y ;
PERACCHIA, MT ;
TRUBETSKOY, V ;
TORCHILIN, V ;
LANGER, R .
SCIENCE, 1994, 263 (5153) :1600-1603
[73]   INCORPORATION OF CAROTENOIDS IN AQUEOUS SYSTEMS - UPTAKE BY CULTURED RAT HEPATOCYTES [J].
GROLIER, P ;
AZAISBRAESCO, V ;
ZELMIRE, L ;
FESSI, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1111 (01) :135-138
[74]   Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs [J].
Gursoy, RN ;
Benita, S .
BIOMEDICINE & PHARMACOTHERAPY, 2004, 58 (03) :173-182
[75]   THE EFFECT OF LIPID EMULSIONS ON RETICULOENDOTHELIAL SYSTEM FUNCTION IN THE INJURED ANIMAL [J].
HAMAWY, KJ ;
MOLDAWER, LL ;
GEORGIEFF, M ;
VALICENTI, AJ ;
BABAYAN, VK ;
BISTRIAN, BR ;
BLACKBURN, GL .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 1985, 9 (05) :559-565
[76]   EFFECTS OF CHOLESTEROL AND CHOLESTERYL OLEATE ON LIPOLYSIS AND LIVER UPTAKE OF TRIGLYCERIDE/PHOSPHATIDYLCHOLINE EMULSIONS IN RATS [J].
HANDA, T ;
EGUCHI, Y ;
MIYAJIMA, K .
PHARMACEUTICAL RESEARCH, 1994, 11 (09) :1283-1287
[77]  
Hara T, 1995, GENE THER, V2, P784
[78]   Emulsion formulations as a vector for gene delivery in vitro and in vivo [J].
Hara, T ;
Liu, F ;
Liu, DX ;
Huang, L .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 24 (2-3) :265-271
[79]   In vivo gene delivery to the liver using reconstituted chylomicron remnants as a novel nonviral vector [J].
Hara, T ;
Tan, Y ;
Huang, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14547-14552
[80]   Adsorption kinetics of plasma proteins on oil-in-water emulsions for parenteral nutrition [J].
Harnisch, S ;
Müller, RH .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2000, 49 (01) :41-46