优化 5-氟尿嘧啶弹性脂质体经皮给药的渗透促进剂:设计专家第二部分。

Optimized permeation enhancer for topical delivery of 5-fluorouracil-loaded elastic liposome using Design Expert: part II.

机构信息

a Department of Pharmaceutical Sciences and Technology , Birla Institute of Technology , Ranchi , Jharkhand , India and.

b Department of Pharmaceutics , Jamia Hamdard (Hamdard University) , New Delhi , India.

出版信息

Drug Deliv. 2016 May;23(4):1242-53. doi: 10.3109/10717544.2015.1124473. Epub 2015 Dec 24.

Abstract

OBJECTIVE

To prepare and optimize the topical elastic liposome (EL)-loaded carbopol-980 gel of 5-Fluorouracil (5-FU) containing permeation enhancers (azone, propylene glycol (PG) and lauryl alcohol (LA)) and further evaluation for permeation flux of 5-FU, the activation energy and irritation in the rat skin.

METHODS

EL formulations were prepared using phosphatidylcholine and varied surfactants (Span 60, Span 80 and Tween-80) by rotator evaporation method and optimized by experimental design. In vitro characterizations dictated the EL containing Span 80 (lipid:surfactant = 7:3) (EL3-S80) for further optimization of gel. Different gel formulations (5% w/w) with varying concentration (1-3%) of permeation enhancers were prepared and evaluated for viscosity, spreadability, the 5-FU permeation and deposition. The activation energy using the Franz diffusion cell and the plausible irritation using the Draize test were assessed on the albino rat and rabbit, respectively.

RESULTS AND DISCUSSION

EL3-S80 was selected as an optimized EL owing to maximum desirability (0.99) and enhanced 5-FU flux (187.86 ± 14.1 μg/cm(2)/h). EL3-S80 suspension loaded gels (0.5%) revealed reduced viscosity leading to higher spreadability than blank gel. EL containing 3% azone in gel, EL containing 3% LA in gel and EL containing 3% PG in gel portrayed 187.86 ± 14.1, 117.7 ± 13.4 and 106.7 ± 7.3 μg/cm(2)/h as enhanced 5-FU flux values, respectively as compared to drug solution (8.8 ± 0.76 μg/cm(2)/h). Furthermore, reduced value of activation energy (2.63-folds) and the non-irritancy of gel could be effective and safe.

CONCLUSION

ELA-3 gel formulation could be used as an effective and economic gel in cutaneous cancer and skin-related keratoses.

摘要

目的

制备并优化载有 5-氟尿嘧啶(5-FU)的透皮促进剂(氮酮、丙二醇(PG)和月桂醇(LA))的局部弹性脂质体(EL)/卡波姆 980 凝胶,并进一步评价其在大鼠皮肤中的 5-FU 渗透通量、激活能和刺激性。

方法

采用旋转蒸发法,以磷脂和不同表面活性剂(Span 60、Span 80 和 Tween-80)制备 EL 制剂,并通过实验设计进行优化。体外特性研究表明,含有 Span 80(脂质:表面活性剂=7:3)的 EL(EL3-S80)适合进一步优化凝胶。制备了不同浓度(1-3%)透皮促进剂的 5%w/w 凝胶,并对其粘度、铺展性、5-FU 渗透和沉积进行了评价。Franz 扩散池评估激活能,Draize 试验评估潜在刺激性,分别在白化大鼠和兔上进行。

结果与讨论

EL3-S80 被选为最佳 EL,因为其最大理想性(0.99)和增强的 5-FU 通量(187.86±14.1μg/cm2/h)。EL3-S80 混悬液负载凝胶(0.5%)的粘度降低,铺展性提高,优于空白凝胶。载有 3%氮酮的 EL 凝胶、载有 3%月桂醇的 EL 凝胶和载有 3%PG 的 EL 凝胶的 5-FU 渗透通量分别为 187.86±14.1μg/cm2/h、117.7±13.4μg/cm2/h和 106.7±7.3μg/cm2/h,与药物溶液(8.8±0.76μg/cm2/h)相比,均有显著增强。此外,激活能值降低(2.63 倍)和凝胶无刺激性,可能是有效和安全的。

结论

ELA-3 凝胶制剂可作为治疗皮肤癌和皮肤相关角化病的有效、经济的凝胶制剂。

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