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Solid Lipid Nanoparticles for Topical Drug Delivery: Mechanisms, Dosage Form Perspectives, and Translational Status

机译:用于局部药物递送的固体脂质纳米颗粒:机制,剂型形式的观点,以及平移状态

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摘要

Solid lipid nanoparticles (SLNs) have shown potential as a novel lipid-based drug delivery system the topical applications of innumerable therapeutic compounds. However, the mechanisms governing the absorption and cellular uptake of SLNs through topical route, along with the mechanism of drug release from SLNs still ambiguous, and require further investigation. In addition, the selection of an appropriate dosage form/formulation base is essential for ease of application of SLNs and to enhance dermal and transdermal delivery. Upscaling and regulatory approvals are other challenges that may impede the clinical translation of SLNs. Therefore, this review focusses on different mechanisms involved in skin penetration and cellular uptake of SLNs. This is followed by a comprehensive discussion on the physicochemical properties of SLNs including various formulation and dosage form factors, which might influence the absorption of SLNs through the skin. Finally, translational status with respect to scale-up and regulatory aspects are also discussed. This review will be useful to researchers with an interest in topical applications of SLNs for the efficient delivery of drugs and cosmetics.
机译:固体脂质纳米颗粒(SLNS)显示出作为新型脂质的药物递送系统的潜力,其局部应用无数治疗化合物。然而,通过局部途径的吸收和细胞吸收的机制,以及SLNS仍然模糊的药物释放机制,需要进一步调查。此外,选择适当的剂型/配方碱对于易于施加SLN并增强皮肤和透皮递送至关重要。升级和监管审批是其他可能阻碍SLN的临床翻译的其他挑战。因此,本综述侧重于涉及皮肤渗透和蜂窝摄取的不同机制。随后是关于SLN的物理化学特性的综合讨论,包括各种配方和剂型因子,这可能影响通过皮肤的SLNS的吸收。最后,还讨论了扩展和监管方面的平移地位。本综述对研究人员对SLNS的局部应用兴趣有益,以便有效地提供药物和化妆品。

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