Development and Optimization of Nanoemulsion from Ethanolic Extract of Centella asiatica (NanoSECA) Using D-Optimal Mixture Design to Improve Blood-Brain Barrier Permeability

被引:16
|
作者
Jusril, Nor Atiqah [1 ]
Abu Bakar, Syahrul Imran [1 ,2 ]
Khalil, Khalilah Abdul [1 ]
Md Saad, Wan Mazlina [3 ]
Wen, Ng Kwok [4 ]
Adenan, Mohd Ilham [1 ,5 ]
机构
[1] Univ Teknologi MARA, Fac Sci Appl, Shah Alam 40450, Selangor, Malaysia
[2] Atta ur Rahman Inst Nat Product Discovery AuRIns, Level 9, Puncak Alam Campus, Puncak Alam 42300, Selangor, Malaysia
[3] Univ Teknologi MARA, Ctr Med Lab Technol, Fac Hlth Sci, Puncak Alam 42300, Selangor, Malaysia
[4] Quest Int Univ, Fac Pharm, Jalan Raja Permaisuri Bainun, Ipoh 30250, Perak, Malaysia
[5] Univ Teknologi MARA Pahang Branch, Bandar Pusat Jengka 26400, Pahang, Malaysia
关键词
DRUG-DELIVERY; FORMULATION; OIL; STABILITY; ACID; PHARMACOKINETICS; SYSTEM; MEMORY; RATS;
D O I
10.1155/2022/3483511
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
The evidence on the neuroprotective impact of Centella asiatica (C. asiatica) has been greatly documented in recent years. However, a major obstacle that remains to be overcome is the capacity of the active molecules in C. asiatica to cross the blood-brain barrier (BBB). In this study, we explored the possibilities of using a D-optimal mixture design to fabricate nanoemulsion of C. asiatica (NanoSECA) for better brain bioavailability. The parameters for optimization were the percentage of water (10-80% w/v) and virgin coconut oil (VCO) (10-80% w/v). Nanoemulsions were formulated using a high-pressure homogenization approach and were characterized for their physicochemical properties. The optimal VCO-based nanoemulsion (VBN: F2) conditions were found at 80% (w/v) of water and 10% (w/v) of VCO. Subsequently, viability tests were conducted on neuroblastoma (SH-SY5Y) and macrophage (RAW 264.7) cell lines. NanoSECA was distinguished for its antioxidant, acetylcholinesterase (AChE), anti-inflammatory, and parallel artificial membrane permeability assay (PAMPA) activities in vitro. The NanoSECA has a particle size of 127.833 +/- 8.280 nm, zeta potential (ZP) of -24.9 +/- 0.011 mV, polydispersity index (PDI) of 0.493 +/- 4.681, percentage prediction error (PPE) of -12.02%, and pH of 6.0 +/- 0.006 and is also stable under different storage conditions. Cell viability was improved in a dose-dependent manner on SH-SY5Y and RAW 264.7 cell lines. In addition, NanoSECA significantly reduced the AChE activity, suppressing the level of proinflammatory mediators and oxidative stress. Moreover, NanoSECA showed high BBB permeation with a high value of experimental permeability to cross the BBB. Thus, NanoSECA could efficiently potentiate the central nervous system (CNS) therapeutic activities through enhanced penetration of BBB. These nano-delivery systems are crucial to unlock the full potential of C. asiatica for treating numerous CNS disorders.
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页数:18
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