Development and characterization of a nano-drug delivery system containing vasaka phospholipid complex to improve bioavailability using quality by design approach

被引:19
|
作者
Sundaresan, Nandhini [1 ]
Kaliappan, Ilango [1 ,2 ]
机构
[1] SRM Inst Sci & Technol, Interdisciplinary Inst Indian Syst Med IIISM, Div Pharmacognosy & Phytochem, Chengalpattu Dt 603203, Tamil Nadu, India
[2] SRM Inst Sci & Technol, SRM Coll Pharm, Dept Pharmaceut Chem, Chengalpattu Dt 603203, Tamil Nadu, India
关键词
Adhatoda vasica; Box Behnken design; Phosphatidylcholine; Phytosome; Vasicine; ADHATODA-VASICA; OPTIMIZATION; ENHANCEMENT; LIPOSOMES; CARRIERS;
D O I
10.4103/1735-5362.305193
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background and purpose: Vasicine is a potential bronchodilator and can be used for the effective management of asthma and bronchitis. It has low absorption in the gastrointestinal tract due to its poor solubility thereby low bioavailability. The objective of this research was to develop a novel drug delivery system of vasaka extract to improve its bioavailability by enhancing the solubility and absorption of vasicine. Experimental approach: Vasaka-loaded phytosomes were developed and optimized by thin-layer hydration technique using systematic quality by design approach. Box-Behnken design (32 factorial design) using Design-Expert software was employed to optimize phytosome wherein phosphatidylcholine concentration (X1), stirring temperature (X2), and stirring time (X3) were selected as independent variables. Yield (%), particle size (nm), and entrapment efficiency (%) were evaluated as responses. The optimized phytosome was characterized by studying the surface morphology such as FE-SEM and TEM analysis, thermal characteristics by thermal gravimetric analysis and spectral and diffraction studies by FTIR and XRD analysis and studying the dissolution behaviour of phytosome by in vitro release study. Findings/Results: The percentage yield, particle size, and entrapment efficiency values of the phytosomes were found in the range of 30.03-97.03%, 231.0-701.4 nm, and 20.02-95.88% w/w, respectively. The optimized phytosome showed the zeta potential of -23.2 mV exhibited good stability and SEM and TEM analysis revealed the spherical shape and smooth particles with the uniform particle size distribution of phytosomes. The comparative in vitro drug release study of vasaka extract and phytosome revealed the sustained release characteristics of phytosome which reached 68.80% at 8 h compared to vasaka extract reached a maximum of 45.08% at 4 h. Conclusion and implication: The results highlighted the importance of optimization of formulation development using quality by design strategy to achieve consistent quality of pharmaceutical products.
引用
收藏
页码:103 / 117
页数:15
相关论文
共 50 条
  • [1] Development and characterization of a multiparticulate drug delivery system containing indomethacin-phospholipid complex to improve dissolution rate
    Kaffash, Ehsan
    Badiee, Ali
    Akhgari, Abbas
    Rezayat, Negar Akhavan
    Abbaspour, Mohammadreza
    Saremnejad, Farinaz
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2019, 53
  • [2] Development of phospholipid complex loaded self-microemulsifying drug delivery system to improve the oral bioavailability of resveratrol
    Luo, Xinxin
    Wang, Dandan
    Wang, Min
    Deng, Suya
    Huang, Yike
    Xia, Zhining
    NANOMEDICINE, 2021, 16 (09) : 721 - 740
  • [3] Recent Development of Copolymeric Nano-Drug Delivery System for Paclitaxel
    Chen, Shiyu
    Song, Zhimei
    Feng, Runliang
    ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2020, 20 (18) : 2169 - 2189
  • [4] Nano-drug delivery system: a promising approach against breast cancer
    Malik, Jonaid Ahmad
    Ansari, Jeba Ajgar
    Ahmed, Sakeel
    Khan, Afreen
    Ahemad, Nafees
    Anwar, Sirajudheen
    THERAPEUTIC DELIVERY, 2023, 14 (05) : 357 - 381
  • [5] Bioavailability Enhancement of Polymyxin B With Novel Drug Delivery: Development and Optimization Using Quality-by-Design Approach
    Chauhan, Meenakshi K.
    Bhatt, Nidhi
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 108 (04) : 1521 - 1528
  • [6] DEVELOPMENT OF PLGA-PEG BASED NANO-DRUG DELIVERY SYSTEM FOR CYSTIC FIBROSIS
    Vij, N.
    Ding, H.
    Mazur, S.
    Roy, I
    PEDIATRIC PULMONOLOGY, 2009, : 298 - 298
  • [7] In vivo Toxicity Evaluation of a Nano-drug Delivery System Using a Caenorhabditis elegans Model System
    Han Wenzhao
    Li Hui
    Yu Xiaoxuan
    Ke Junfeng
    Guo Feng
    Wang Liping
    CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2022, 38 (04) : 1018 - 1024
  • [8] In vivo Toxicity Evaluation of a Nano-drug Delivery System Using a Caenorhabditis elegans Model System
    Wenzhao Han
    Hui Li
    Xiaoxuan Yu
    Junfeng Ke
    Feng Guo
    Liping Wang
    Chemical Research in Chinese Universities, 2022, 38 : 1018 - 1024
  • [9] Development of sorafenib loaded nanoparticles to improve oral bioavailability using a quality by design approach
    Park, Sang Yeob
    Kang, Zion
    Thapa, Prakash
    Jin, Yong Suk
    Park, Joo Won
    Lim, Hye Jung
    Lee, Jae Young
    Lee, Sa-Won
    Seo, Min-Hyo
    Kim, Min-Soo
    Jeong, Seong Hoon
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2019, 566 : 229 - 238
  • [10] Peptide-Conjugated Nano-Drug Delivery System to Improve Synergistic Molecular Chemotherapy for Colon Carcinoma
    Rayappan, Kathirvel
    Murugan, Chandran
    Sundarraj, Shenbagamoorthy
    Lara, Roberto Portillo
    Kannan, Soundarapandian
    CHEMISTRYSELECT, 2017, 2 (27): : 8524 - 8534