In VitroEvaluation of Curcumin-Encapsulated Chitosan Nanoparticles against Feline Infectious Peritonitis Virus and Pharmacokinetics Study in Cats

被引:19
作者
Ng, Shing Wei [1 ]
Selvarajah, Gayathri Thevi [1 ,2 ]
Hussein, Mohd Zobir [3 ]
Yeap, Swee Keong [4 ]
Omar, Abdul Rahman [1 ,5 ]
机构
[1] Univ Putra Malaysia, Inst Biosci, Upm Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Fac Vet Med, Dept Vet Clin Studies, Upm Serdang 43400, Selangor, Malaysia
[3] Univ Putra Malaysia, Inst Adv Technol, Lab Mat Synth & Characterizat, Upm Serdang 43400, Selangor, Malaysia
[4] Xiamen Univ Malaysia, China ASEAN Marine Sci Sch, Sepang, Selangor, Malaysia
[5] Univ Putra Malaysia, Fac Vet Med, Dept Pathol & Microbiol, Upm Serdang 43400, Selangor, Malaysia
关键词
ANTIBODY-DEPENDENT ENHANCEMENT; ORAL BIOAVAILABILITY; ANTIVIRAL ACTIVITY; MOLECULAR-WEIGHT; BURST RELEASE; CORONAVIRUS; DELIVERY; EXPRESSION; MICROPARTICLES; FORMULATION;
D O I
10.1155/2020/3012198
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Feline infectious peritonitis (FIP) is an important feline viral disease, causing an overridden inflammatory response that results in a high mortality rate, primarily in young cats. Curcumin is notable for its biological activities against various viral diseases; however, its poor bioavailability has hindered its potential in therapeutic application. In this study, curcumin was encapsulated in chitosan nanoparticles to improve its bioavailability. Curcumin-encapsulated chitosan (Cur-CS) nanoparticles were synthesised based on the ionic gelation technique and were spherical and cuboidal in shape, with an average particle size of 330 nm and +42 mV in zeta potential. The nanoparticles exerted lower toxicity in Crandell-Rees feline kidney (CrFK) cells and enhanced antiviral activities with a selective index (SI) value three times higher than that of curcumin. Feline-specific bead-based multiplex immunoassay and qPCR were used to examine their modulatory effects on proinflammatory cytokines, including tumour necrosis factor (TNF)alpha, interleukin- (IL-) 6, and IL-1 beta. There were significant decrements in IL-1 beta, IL-6, and TNF alpha expression in both curcumin and Cur-CS nanoparticles. Based on the multiplex immunoassay, curcumin and the Cur-CS nanoparticles could lower the immune-related proteins in FIP virus (FIPV) infection. The single- and multiple-dose pharmacokinetics profiles of curcumin and the Cur-CS nanoparticles were determined by high-performance liquid chromatography (HPLC). Oral delivery of the Cur-CS nanoparticles to cats showed enhanced bioavailability with a maximum plasma concentration (Cmax) value of 621.5 ng/mL. Incorporating chitosan nanoparticles to deliver curcumin improved the oral bioavailability and antiviral effects of curcumin against FIPV infection. This study provides evidence for the potential of Cur-CS nanoparticles as a supplementary treatment of FIP.
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页数:18
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