College of Pharmacy, Hanyang University, 55 Hanyangdaehak-ro, Sangnok-gu, Ansan 15588, South Korea.
Department of Pharmacy, Quaid-I-Azam University, Islamabad 45320, Pakistan.
Int J Pharm. 2021 Jan 5;592:120039. doi: 10.1016/j.ijpharm.2020.120039. Epub 2020 Nov 2.
The purpose of this study was to compare two types of emulsification techniques in a solid self-nanoemulsifying drug delivery system (SNEDDS); high-pressure homogenisation (HPH) and Shirasu porous glass membrane (SPG). Those two emulsification processes enhanced the solubility, dissolution and oral bioavailability of poorly water-soluble sildenafil base (SB) by producing fine and well-dispersed nanoemulsion droplet. The liquid SNEDDS consisting of Labrasol/Transcutol HP/coconut oil at the weight of 72/18/10, gave the smallest emulsion droplet size among the prepared liquid SNEDDS formulations. Then, the SB-loaded liquid SNEDDS was dissolved in the deionised water and applied to HPH or SPG techniques. Aerosil 200 was suspended as a mesoporous carrier and spray-dried, producing an SB-loaded solid SNEDDS. The emulsion droplet size, solubility and dissolution of each emulsification process were compared to the solid SNEDDS fabricated without any treatment of additional emulsification. Moreover, the physicochemical properties of all formulations were compared. The crystalline state of the drug in all products was converted to the amorphous state. The solid SNEDDS, subjected to HPH technique, provided fine and well-dispersed nanoemulsion. Additionally, it increasingly improved the drug solubility and dissolution as compared to the others, including SB powder, non-treated (NT) and SPG. Furthermore, it gave improved C and increased AUC compared to SB powder and SPG, indicating HPH enhanced the oral bioavailability of SB the most. Thus, this solid SNEDDS with HPH would be strongly suggested as an oral SB-loaded pharmaceutical product.
本研究旨在比较两种乳化技术在固体自微乳给药系统(SNEDDS)中的应用:高压均质(HPH)和 Shirasu 多孔玻璃膜(SPG)。这两种乳化工艺通过产生细小且分散良好的纳米乳液滴,提高了难溶性西地那非碱(SB)的溶解度、溶解速率和口服生物利用度。由 Labrasol/Transcutol HP/椰子油组成的重量比为 72/18/10 的液态 SNEDDS 制剂具有最小的乳液液滴尺寸。然后,将载有 SB 的液态 SNEDDS 溶解在去离子水中,并应用于 HPH 或 SPG 技术。Aerosil 200 被用作中孔载体并进行喷雾干燥,从而产生载有 SB 的固态 SNEDDS。比较了每种乳化工艺的乳液液滴尺寸、溶解度和溶解速率与未经过任何额外乳化处理的固态 SNEDDS。此外,还比较了所有制剂的物理化学性质。药物在所有产品中的晶型均转化为无定形态。经 HPH 处理的固态 SNEDDS 提供了细小且分散良好的纳米乳液。此外,与其他制剂(包括 SB 粉末、未经处理的(NT)和 SPG)相比,它显著提高了药物的溶解度和溶解速率。此外,它与 SB 粉末和 SPG 相比,增加了 C 和 AUC,表明 HPH 最能提高 SB 的口服生物利用度。因此,建议将具有 HPH 的这种固态 SNEDDS 作为 SB 的口服载药制剂。