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3D 打印、控释、三联抗 HIV-1 治疗片剂基质用于高级抗 HIV-1 药物输送。

3D printed, controlled release, tritherapeutic tablet matrix for advanced anti-HIV-1 drug delivery.

机构信息

Wits Advanced Drug Delivery Platform Research Unit, Department of Pharmacy and Pharmacology, School of Therapeutic Sciences, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, 7 York Road, Parktown 2193, South Africa.

Wits Advanced Drug Delivery Platform Research Unit, Department of Pharmacy and Pharmacology, School of Therapeutic Sciences, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, 7 York Road, Parktown 2193, South Africa.

出版信息

Eur J Pharm Biopharm. 2019 May;138:99-110. doi: 10.1016/j.ejpb.2018.04.007. Epub 2018 Apr 12.

Abstract

PURPOSE

A 3D-Bioplotter® was employed to 3D print (3DP) a humic acid-polyquaternium 10 (HA-PQ10) controlled release fixed dose combination (FDC) tablet comprising of the anti-HIV-1 drugs, efavirenz (EFV), tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC).

METHODS

Chemical interactions, surface morphology and mechanical strength of the FDC were ascertained. In vitro drug release studies were conducted in biorelevant media followed by in vivo study in the large white pigs, in comparison with a market formulation, Atripla®. In vitro-in vivo correlation of results was undertaken.

RESULTS

EFV, TDF and FTC were successfully entrapped in the 24-layered rectangular prism-shaped 3DP FDC with a loading of ∼12.5 mg/6.3 mg/4 mg of EFV/TDF/FTC respectively per printed layer. Hydrogen bonding between the EFV/TDF/FTC and HA-PQ10 was detected which was indicative of possible drug solubility enhancement. The overall surface of the tablet exhibited a fibrilla structure and the 90° inner pattern was determined to be optimal for 3DP of the FDC. In vitro and in vivo drug release profiles from the 3DP FDC demonstrated that intestinal-targeted and controlled drug release was achieved.

CONCLUSION

A 3DP FDC was successfully manufactured with the aid of a 3D-Bioplotter in a single step process. The versatile HA-PQ10 entrapped all drugs and achieved an enhanced relative bioavailability of EFV, TDF, and FTC compared to the market formulation for potentially enhanced HIV treatment.

摘要

目的

使用 3D 生物打印机(3DP)打印包含抗 HIV-1 药物依非韦伦(EFV)、富马酸替诺福韦二吡呋酯(TDF)和恩曲他滨(FTC)的腐殖酸-聚季铵盐 10(HA-PQ10)控释固定剂量组合(FDC)片剂,以实现 3DP。

方法

确定了 FDC 的化学相互作用、表面形貌和机械强度。在生物相关介质中进行了体外药物释放研究,然后在大型白猪中进行了体内研究,并与市场制剂 Atripla®进行了比较。进行了体外-体内相关性研究。

结果

成功地将 EFV、TDF 和 FTC 包埋在 24 层矩形棱柱形 3DP FDC 中,每层打印的 EFV/TDF/FTC 负载约为 12.5mg/6.3mg/4mg。检测到 EFV/TDF/FTC 与 HA-PQ10 之间的氢键相互作用,这表明可能增强了药物的溶解度。片剂的整体表面呈现出纤维状结构,确定 90°内角图案是 3DP FDC 的最佳图案。3DP FDC 的体外和体内药物释放曲线表明,实现了肠道靶向和控释药物释放。

结论

借助 3D 生物打印机,成功地一步法制造了 3DP FDC。多功能的 HA-PQ10 包埋了所有药物,并与市场制剂相比,提高了 EFV、TDF 和 FTC 的相对生物利用度,可能增强了 HIV 治疗效果。

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