Bioactive Self-Nanoemulsifying Drug Delivery Systems (Bio-SNEDDS) for Combined Oral Delivery of Curcumin and Piperine

被引:53
|
作者
Kazi, Mohsin [1 ,2 ]
Shahba, Ahmad A. [2 ]
Alrashoud, Saad [1 ]
Alwadei, Majed [1 ]
Sherif, Abdelrahman Y. [1 ]
Alanazi, Fars K. [1 ,2 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut, Riyadh 11451, Saudi Arabia
[2] King Saud Univ, Dept Pharmaceut, Coll Pharm, Kayyali Chair Pharmaceut Ind, Riyadh 11451, Saudi Arabia
来源
MOLECULES | 2020年 / 25卷 / 07期
关键词
curcumin and piperine; combination therapy; solidification technique; self-nanoemulsifying drug delivery systems (SNEDDS); dissolution improvement; bio-SNEDDS; LIPID-BASED FORMULATIONS; BED COATING PREPARATION; IN-VITRO; OXIDATIVE STRESS; NIGELLA-SATIVA; SOLID SEDDS; DESIGN; OPTIMIZATION; DISSOLUTION; BIOAVAILABILITY;
D O I
10.3390/molecules25071703
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Bioactive oils of natural origin have gained huge interests from health care professionals and patients. Objective: To design a bioactive self-nanoemulsifying drug delivery system (Bio-SNEDDS) comprising curcumin (CUR) and piperine (PP) by incorporating bioactive natural oils in the formulation. Methods: The self-emulsifying properties of apricot, avocado, black seed and Zanthoxylum rhetsa seed oils were screened within various SNEDDS formulations. Each liquid SNEDDS formulation was loaded with both CUR and PP. The optimal liquid SNEDDS were solidified using Aeroperl((R)) and Neusilin((R)) at 1:1 w/w ratio. Liquid and solid SNEDDS were characterized by droplet size analysis, equilibrium solubility, scanning electron microscopy, X-ray powder diffraction, differential scanning calorimetry, and Fourier transform infrared spectroscopy. In-vitro dissolution studies were performed to evaluate the efficiency of CUR and PP release from solid Bio-SNEDDS. Results: The liquid SNEDDS comprised of black seed oil exhibited excellent self-emulsification performance, low droplet size along with transparent appearance. The inclusion of the cosolvent Transcutol P improved the solubilization capacity of both CUR and PP. The liquid SNEDDS were efficiently solidified using the two adsorbents and presented the drugs within amorphous state. In particular, SNEDDS comprised of black seed oil/Imwitor988/Transcutol P/Cremophor RH40 (20/20/10/50) and when solidified with Neusilin showed enhanced CUR and PP release (up to 60% and 77%, respectively). In addition, this formulation efficiently delivers the highly bioactive black seed oil to the patient. Conclusions: The optimized Bio-SNEDDS comprising black seed oil showed outstanding self-emulsification characteristics along with enhanced CUR/PP dissolution upon solidification.
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页数:24
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