Department of Pharmaceutics, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Paud Road, Rambaug Colony, Erandwane, Pune, Maharashtra, 411038, India.
AAPS PharmSciTech. 2020 Oct 9;21(7):279. doi: 10.1208/s12249-020-01801-1.
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.
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。