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负载枸橼酸西地那非并包含在口服冻干速溶片中的自纳米乳化系统:制备、优化及体内评价

Self-Nanoemulsifying System Loaded with Sildenafil Citrate and Incorporated within Oral Lyophilized Flash Tablets: Preparation, Optimization, and In Vivo Evaluation.

作者信息

Hosny Khaled M, Alhakamy Nabil A, Almodhwahi Maeen A, Kurakula Mallesh, Almehmady Alshaimaa M, Elgebaly Samar S

机构信息

Department of Pharmaceutics, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.

Center of Excellence for Drug Research and Pharmaceutical Industries, King Abdulaziz University, Jeddah 21589, Saudi Arabia.

出版信息

Pharmaceutics. 2020 Nov 21;12(11):1124. doi: 10.3390/pharmaceutics12111124.

Abstract

Sildenafil citrate is a drug used throughout the world primarily to treat erectile dysfunction. Several problems with the commercially available product decrease its efficacy, such as limited solubility, delayed onset of action, and low bioavailability with a large variability in the absorption profile. This study aimed to develop an optimized self-nanoemulsifying lyophilized tablet for the drug to conquer the foresaid problems. Sildenafil solubility in various surfactants, oils, and cosurfactants was attempted. An optimized formulation of a loaded self-nanoemulsion with a small droplet size was developed by applying a special cubic model of the mixture design. Sixteen formulations were prepared and characterized for droplet size. On the basis of solubility studies, a clove oil/oleic acid mixture, polysorbate 20 (Tween 20), and propylene glycol were selected as the proposed oil, surfactant, and cosurfactant, respectively. On the basis of desirability, an optimized sildenafil citrate-loaded self-nanoemulsifying delivery system containing 10% of the oil mixture, 60% of the surfactant, and 30% of the cosurfactant had a droplet size of 65 nm. Subsequently, the tablet form was fabricated with optimum ratios of 0.4% fumed silica, 0.1% hydroxypropyl methylcellulose, and 0.4% sodium starch glycolate. This formula showed satisfactory results in both disintegration and dissolution studies. In vivo pharmacokinetic studies indicated a higher bioavailability (1.44 times) and rapid absorption profile for the study's tablets compared with commercially available tablets. In conclusion, highly bioavailable oral lyophilized flash tablets of sildenafil were successfully prepared. They will be a good alternative to the conventional solid-dosage form.

摘要

枸橼酸西地那非是一种在全球主要用于治疗勃起功能障碍的药物。市售产品存在的一些问题降低了其疗效,如溶解度有限、起效延迟以及生物利用度低且吸收情况差异大。本研究旨在开发一种优化的自纳米乳化冻干片来解决上述问题。尝试了西地那非在各种表面活性剂、油和助表面活性剂中的溶解度。通过应用混合设计的特殊立方模型,开发了一种具有小液滴尺寸的负载型自纳米乳剂的优化配方。制备了16种配方并对液滴尺寸进行了表征。基于溶解度研究,分别选择丁香油/油酸混合物、聚山梨酯20(吐温20)和丙二醇作为拟用的油、表面活性剂和助表面活性剂。基于可取性,一种含有10%油混合物、60%表面活性剂和30%助表面活性剂的优化的负载枸橼酸西地那非的自纳米乳化给药系统的液滴尺寸为65nm。随后,用0.4%的气相二氧化硅、0.1%的羟丙基甲基纤维素和0.4%的淀粉乙醇酸钠的最佳比例制备片剂。该配方在崩解和溶出度研究中均显示出令人满意的结果。体内药代动力学研究表明,与市售片剂相比,该研究中的片剂具有更高的生物利用度(1.44倍)和快速吸收情况。总之,成功制备了具有高生物利用度的口服西地那非冻干速溶片。它们将是传统固体剂型的良好替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0777/7700536/a843ce7c5fc9/pharmaceutics-12-01124-g001a.jpg

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