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在非人灵长类动物中,给予一剂包含洛匹那韦、依非韦伦和替诺福韦的三合一纳米混悬剂后,细胞和血浆中的药物水平延长。

Extended cell and plasma drug levels after one dose of a three-in-one nanosuspension containing lopinavir, efavirenz, and tenofovir in nonhuman primates.

机构信息

Department of Pharmaceutics.

Department of Medicine.

出版信息

AIDS. 2018 Nov 13;32(17):2463-2467. doi: 10.1097/QAD.0000000000001969.

Abstract

OBJECTIVE

To characterize a drug-combination nanoparticle (DcNP) containing water-insoluble lopinavir (LPV) and efavirenz (EFV), and water-soluble tenofovir (TFV), for its potential as a long-acting combination HIV treatment.

DESIGN

Three HIV drugs (LPV, EFV, TFV) with well established efficacy and safety were coformulated into a single DcNP suspension. Two macaques were administered one subcutaneous injection and drug concentrations in plasma and mononuclear cells (in peripheral blood and lymph nodes) were analyzed over 2 weeks. Pharmacokinetic parameters and cell-to-plasma relationships of LPV, EFV, and TFV were determined.

RESULTS

This three-in-one nanoformulation provided extended concentrations of all drugs in lymph node cells that were 57- to 228-fold higher than those in plasma. Levels of all three drugs in peripheral blood mononuclear cells persisted for 2 weeks at levels equal to or higher than those in plasma.

CONCLUSION

With long-acting characteristics and higher drug penetration/persistence in cells, this three-in-one DcNP may enhance therapeutic efficacy of these well studied HIV drugs due to colocalization and targeting of this three-drug combination to HIV host cells.

摘要

目的

描述一种载有脂溶性洛匹那韦(LPV)和依非韦伦(EFV)及水溶性替诺福韦(TFV)的药物组合纳米颗粒(DcNP),以评估其作为长效抗 HIV 治疗组合的潜力。

设计

将三种具有明确疗效和安全性的 HIV 药物(LPV、EFV、TFV)共同配制在单一 DcNP 混悬液中。对两只猕猴进行了一次皮下注射,在 2 周内分析了血浆和单核细胞(外周血和淋巴结)中的药物浓度。测定了 LPV、EFV 和 TFV 的药代动力学参数和细胞-血浆关系。

结果

这种三合一纳米制剂可使淋巴结细胞中所有药物的浓度延长,比血浆中的浓度高 57-228 倍。外周血单个核细胞中所有三种药物的浓度在 2 周内持续存在,其水平与血浆中的水平相等或更高。

结论

由于这种三药组合能实现药物共定位和靶向作用,三合一 DcNP 具有长效作用特点和更高的药物穿透/细胞内持久性,可能会增强这些经深入研究的 HIV 药物的治疗效果。

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