Concanavalin-A Decorated Apremilast Loaded Lipidic Nanocapsules: Appraisal of Lectin-Mediated Targeting for Rheumatoid Arthritis Management

被引:0
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作者
Singh, Neelu [1 ]
Singh, Priya [1 ,2 ]
Mishra, Nidhi [1 ]
Pal, Ravi Raj [1 ]
Parashar, Poonam [1 ,3 ]
Nisha, Raquibun [1 ]
Saraf, Shubhini A. [1 ,4 ]
机构
[1] Cent Univ, Babasaheb Bhimrao Ambedkar Univ Lucknow, Dept Pharmaceut Sci, Vidya Vihar,Raebareli Rd, Lucknow 226025, Uttar Pradesh, India
[2] GITAM Univ, Sch Pharm, Patancheru Mandal, Hyderabad 502329, Telangana, India
[3] Amity Univ Uttar Pradesh, Amity Inst Pharm, Lucknow Campus, Lucknow 226028, India
[4] Natl Inst Pharmaceut Educ & Res NIPER, Transit Campus,NIPER Raebareli,Sarojini Nagar,Near, Lucknow 226002, India
关键词
Rheumatoid arthritis; Lipidic nanocapsules; Autoimmune; Concanavalin-A; Bioavailability enhancement; Lectin targeting; ADJUVANT-INDUCED ARTHRITIS; ORAL DELIVERY; OXIDE NANOPARTICLES; FORMULATION; METHOTREXATE; CURCUMIN; SYSTEMS;
D O I
暂无
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Rheumatoid arthritis (RA) is a persistent inflammatory condition primarily impacting small joints in its early stages and bigger joints in its later stages. Conventional therapy is often encountered with numerous limitations resulting in unsatisfactory clinical outcomes. Hence, probing novel compounds and amalgamating them with nanotechnology may increase efficacy in RA management. Apremilast (Apr), a PDE4 inhibitor, has shown potential for RA management; therefore, the current research focused on developing concanavalin-A (conA) decorated Apr-loaded lipidic nanocapsules (LNCs) employing layer-by-layer techniques using chitosan-conA layering. The developed LNCs were examined in vitro, cell lines, and in vivo animal models. Compared to the pure Apr, the LNCs demonstrated non-cytotoxicity in HEK-293 T cell lines, improved anti-rheumatoid efficacy, and decreased side effects in the complete Freund's adjuvant-induced animal model. Moreover, in vivo pharmacodynamics showed a significant decline in inflammatory parameters (C-reactive protein, adenosine deaminase, rheumatoid factor) and biochemical parameters (erythrocyte sedimentation rate, white/red blood cell count, hemoglobin). Further in vivo, pharmacokinetics revealed an augmented oral bioavailability when related to pure Apr. Thus, the anti-arthritic efficacy of Apr against RA was shown to be promising through the administration of conA-decorated Apr-loaded LNCs. Furthermore, the developed LNCs have the potential to be translated from the bench to the bedside.
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