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二肉豆蔻酰-sn-甘油-3-磷酸甘油钠盐(DMPG-Na)与不同金属阳离子的纳米脂质体前体的研究:在癌症治疗中应用于穿心莲内酯的口服传递。

Investigation of 1,2-Dimyristoyl-sn-Glycero-3-Phosphoglycerol-Sodium (DMPG-Na) Lipid with Various Metal Cations in Nanocochleate Preformulation: Application for Andrographolide Oral Delivery in Cancer Therapy.

机构信息

Department of Pharmaceutics, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Paud Road, Rambaug Colony, Erandwane, Pune, Maharashtra, 411038, India.

出版信息

AAPS PharmSciTech. 2020 Oct 9;21(7):279. doi: 10.1208/s12249-020-01801-1.

Abstract

This study aimed at carrying out a preformulation investigation of nanocochleates (NCs) and develop andrographolide-loaded nanocochleates. Preformulation study comprised of exploring the effect of trivalent and divalent ions on transition temperature (TT) of lipid (DMPG-Na), on particle size (PS), entrapment efficacy (EE), zeta potential (ZP) of NCs, and effect of NCs on change in lipid solubility post-NC formation. Further, the andrographolide-loaded nanocochleates made with CaCl (ANDNCs) were characterized for ZP, PS, EE, X-ray powder diffraction (PXRD), differential scanning calorimetry (DSC), transition electron microscopy (TEM), in vitro release studies, in vitro anticancer potential on the cell line of human breast cancer (MCF-7), in vivo oral pharmacokinetic studies, and tissue distribution in female Wistar rats. Nanocochleates developed with CaCl had a significant reduction in PS (1.78-fold) and ZP (1.38-fold), and elevation of EE (1.17-fold) as compared to AlCl developed NCs. Trivalent ions demonstrated elevation of TT as compared to divalent ions. Spiral-shaped ANDNCs demonstrated ZP, PS, and EE of - 121.46 ± 15.12 mV, 360 ± 47 nm, and 68.12 ± 3.81% respectively. In vitro release study of ANDNCs showed a strong pH-dependent release profile due to hydrogen bonding between NCs and andrographolide (AND). Formulated ANDNCs demonstrated 26.99-fold decrease in IC50 value as compared to free AND. Additionally, the oral bioavailability of AND from ANDNCs improved by 1.81-fold as compared to free AND. Furthermore, ANDNCs showed minimum accumulation within the vital organs such as liver, kidney, and spleen. Briefly, the preformulation study laid a platform for better understanding the NCs and its components. Further, developed ANDNCs revealed superior physiochemical properties to be used as an alternative for a clinical setting.

摘要

本研究旨在对纳米耳蜗(NCs)进行制剂前研究,并开发出载有穿心莲内酯的纳米耳蜗。制剂前研究包括研究三价和二价离子对脂质(DMPG-Na)相变温度(TT)、粒径(PS)、包封效率(EE)、Zeta 电位(ZP)的影响,以及 NCs 形成后对脂质溶解度变化的影响。此外,用 CaCl 制成的载有穿心莲内酯的纳米耳蜗(ANDNCs)的 ZP、PS、EE、X 射线粉末衍射(PXRD)、差示扫描量热法(DSC)、透射电子显微镜(TEM)、体外释放研究、对人乳腺癌(MCF-7)细胞系的体外抗癌潜力、体内口服药代动力学研究以及雌性 Wistar 大鼠的组织分布进行了表征。与用 AlCl 制成的 NCs 相比,用 CaCl 制成的 NCs 的 PS(降低 1.78 倍)和 ZP(降低 1.38 倍)显著降低,而 EE(提高 1.17 倍)升高。与二价离子相比,三价离子可提高 TT。螺旋形 ANDNCs 的 ZP、PS 和 EE 分别为-121.46±15.12 mV、360±47 nm 和 68.12±3.81%。ANDNCs 的体外释放研究表明,由于 NCs 和穿心莲内酯(AND)之间的氢键作用,具有很强的 pH 依赖性释放特性。与游离 AND 相比,配方后的 ANDNCs 的 IC50 值降低了 26.99 倍。此外,与游离 AND 相比,AND 从 ANDNCs 的口服生物利用度提高了 1.81 倍。此外,ANDNCs 在肝、肾和脾等重要器官中的积累最小。简而言之,制剂前研究为更好地理解 NCs 及其成分奠定了基础。此外,开发的 ANDNCs 表现出优越的物理化学性质,可作为临床替代品使用。

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