Pharmacokinetics of Free Oxytetracycline and Oxytetracycline Loaded Cockle Shell Calcium Carbonate-Based Nanoparticle inBALB/cMice

被引:0
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作者
Idris, Sherifat Banke [1 ,2 ]
Abdul Kadir, Arifah [1 ]
Abdullah, Jesse F. F. [3 ]
Ramanoon, Siti-Zubaidah [4 ]
Basit, Muhammad Abdul [1 ,5 ]
Abubakar, Md Zuki Z. A. [1 ]
机构
[1] Univ Putra Malaysia, Fac Vet Med, Dept Vet Preclin Studies, Serdang, Malaysia
[2] Usmanu Danfodiyo Univ, Fac Vet Med, Dept Vet Pharmacol & Toxicol, Sokoto, Nigeria
[3] Univ Putra Malaysia, Fac Vet Med, Dept Vet Clin Studies, Serdang, Malaysia
[4] Univ Putra Malaysia, Fac Vet Med, Dept Farm & Exot Anim Med & Surg, Serdang, Malaysia
[5] Bahauddin Zakariya Univ, Fac Vet Sci, Dept Biosci, Multan, Pakistan
关键词
oxytetracycline; pharmacokinetics; BALB; cmice; calcium carbonate nanoparticle; HPLC; MINERALIZED NANOPARTICLES; FORMULATION; INJECTION; BACTERIA; DELIVERY; RELEASE;
D O I
10.3389/fvets.2020.00270
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The development and utilization of nano-antibiotics is currently gaining attention as a possible solution to antibiotic resistance. The aim of this study was therefore to determine the pharmacokinetics of free oxytetracycline (OTC) and oxytetracycline loaded cockle shell calcium carbonate-based nanoparticle (OTC-CNP) after a single dose of intraperitoneal (IP) administration inBALB/c mice. A total of 100 femaleBALB/cmice divided into two groups of equal number (n= 50) were administered with 10 mg/kg OTC and OTC-CNP, respectively. Blood samples were collected before and post-administration from both groups at time 0, 5, 10, 15, and 30 min and 1, 2, 6, 24, and 48 h, and OTC plasma concentration was quantified using a validated HPLC-UV method. The pharmacokinetic parameters were analyzed using a non-compartment model. TheC(max)values of OTC in OTC-CNP and free OTC treated group were 64.99 and 23.53 mu g/ml, respectively. OTC was detected up to 24 h in the OTC-CNP group as against 1 h in the free OTC group following intraperitoneal administration. In the OTC-CNP group, the plasma elimination rate of OTC was slower while the half-life, the area under the curve, and the volume of the distribution were increased. In conclusion, the pharmacokinetic profile of OTC in the OTC-CNP group differs significantly from that of free OTC. However, further studies are necessary to determine the antibacterial efficacy of OTC-CNP for the treatment of bacterial diseases.
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页数:5
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