An analysis of the microencapsulation of ceftiofur in chitosan particles using the spray drying technology

被引:9
|
作者
Helbling, Ignacio M. [1 ]
Busatto, Carlos A. [1 ]
Karp, Federico [1 ]
Islan, German A. [2 ]
Estenoz, Diana A. [1 ]
Luna, Julio A. [1 ]
机构
[1] Univ Nacl Litoral, CONICET, INTEC, 3450 Guemes, RA-3000 Santa Fe, Argentina
[2] Univ Nacl La Plata, CONICET, CINDEFI, RA-1900 La Plata, Argentina
关键词
Ceftiofur; Spray drying; Microencapsulation; Chitosan; Drug delivery; Mathematical modeling; MULTIPLE INTRAMUSCULAR ADMINISTRATIONS; RANDOMIZED CLINICAL-TRIAL; INTRAMAMMARY TREATMENT; LOADED GELATIN; IN-VIVO; PHARMACOKINETICS; SODIUM; HYDROCHLORIDE; MICROPARTICLES; MICROSPHERES;
D O I
10.1016/j.carbpol.2020.115922
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ceftiofur is a third-generation cephalosporin approved to treat numerous infections in production animals. Its commercial formulations are administered daily due to the mean life time, leading to several inconveniences, like operative challenges and non-uniform plasma levels. The objective of this work was to microencapsulate ceftiofur in chitosan particles using spray drying technology to extend the delivery and consequently reduce the dosage frequency. The effect of formulation factors on particle features was studied using a multilevel factorial design. In addition, ceftiofur thermal stability was assayed by differential scanning calorimetry and microbiological assays. Finally, a pharmacokinetic model was developed to predict theoretical plasma concentration in goats. Results showed that ceftiofur thermal stability increased after microencapsulation, indicating a protective effect of chitosan particles. Besides, MIC, IC50 and inhibition halos against E. coli and S. aureus were similar than those of the commercial product. In addition, suitable plasma levels can be theoretically maintained in goats during 48 h with a single injection. These findings suggest that chitosan microparticles could be a good vehicle for ceftiofur administration.
引用
收藏
页数:12
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