Design and development of bioinspired calcium phosphate nanoparticles of MTX: pharmacodynamic and pharmacokinetic evaluation

被引:7
作者
Pandey, Shweta [1 ]
Mahtab, Asiya [1 ]
Kumar, Vijay [2 ]
Ahmad, Farhan Jalees [1 ]
Verma, Anita Kamra [2 ]
Talegaonkar, Sushama [1 ,3 ]
机构
[1] Jamia Hamdard, Sch Pharmaceut Educ & Res, Dept Pharmaceut, New Delhi, India
[2] Univ Delhi, Kirori Mal Coll, Dept Zool, Nano Biotech Lab, Delhi, India
[3] Delhi Pharmaceut Sci & Res Univ, Dept Pharmaceut, New Delhi, India
关键词
Methotrexate; rheumatoid arthritis; calcium phosphate; nanodelivery; pharmacodynamics; pharmacokinetics; IN-VITRO CHARACTERIZATION; RHEUMATOID-ARTHRITIS; HYDROXYAPATITE NANOPARTICLES; EX-VIVO; DELIVERY; DRUG; METHOTREXATE; EFFICACY; CARRIERS; BONE;
D O I
10.1080/03639045.2019.1602139
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of this investigation is the management of rheumatoid arthritis (RA) by developing methotrexate-loaded calcium phosphate nanoparticles (MTX-CAP-NP) and to evaluate pharmacokinetic and pharmacodynamic behavior in adjuvant induced arthritis model. The nanoparticles were synthesized by wet precipitation method and optimized by Box-Behnken experimental design. MTX-CAP-NPs were characterized by TEM, FTIR, DSC and XRD studies. The particle size, zeta potential and entrapment efficiency of the optimized nanoparticles were found to be 204.90 +/- 64 nm, -11.58 +/- 4.80 mV, and 88.33 +/- 3.74%, respectively. TEM, FTIR, DSC and XRD studies revealed that the developed nanoparticles were nearly spherical in shape and the crystalline structure of CAP-NP was not changed after MTX loading. The pharmacokinetic studies revealed that MTX-CAP-NP enhanced bioavailability of MTX by 2.6-fold when compared to marketed formulation (FOLITRAX-10). Under pharmacodynamic evaluation, arthritic assessment, radiography and histopathology studies revealed that CAP has ability to regenerate cartilage and bone therefore, together with MTX, MTX-CAP-NPs have shown significant reduction in disease progression. The overall work demonstrated that the developed nanodelivery system was well tolerated and more effective than the marketed formulation.
引用
收藏
页码:1181 / 1192
页数:12
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