دورية أكاديمية

Formulation, pharmacokinetics, and antibacterial activity of florfenicol-loaded niosome.

التفاصيل البيبلوغرافية
العنوان: Formulation, pharmacokinetics, and antibacterial activity of florfenicol-loaded niosome.
المؤلفون: Abonashey SG; Department of Biochemistry, Animal Health Research Institute, Dokki, Giza, Egypt., Hassan HAFM; Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt. hatem.hassan@pharma.cu.edu.eg.; School of Life and Medical Sciences, University of Hertfordshire Hosted By Global Academic Foundation, New Administrative Capital, Cairo, Egypt. hatem.hassan@pharma.cu.edu.eg., Shalaby MA; Pharmacology Department, Faculty of Veterinary Medicine, Cairo University, Cairo, Egypt., Fouad AG; Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt., Mobarez E; Department of Biochemistry, Animal Health Research Institute, Dokki, Giza, Egypt., El-Banna HA; Pharmacology Department, Faculty of Veterinary Medicine, Cairo University, Cairo, Egypt.
المصدر: Drug delivery and translational research [Drug Deliv Transl Res] 2024 Apr; Vol. 14 (4), pp. 1077-1092. Date of Electronic Publication: 2023 Nov 13.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Springer Country of Publication: United States NLM ID: 101540061 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2190-3948 (Electronic) Linking ISSN: 2190393X NLM ISO Abbreviation: Drug Deliv Transl Res Subsets: MEDLINE
أسماء مطبوعة: Original Publication: New York : Springer
مواضيع طبية MeSH: Liposomes* , Escherichia coli*, Thiamphenicol/*analogs & derivatives, Animals ; Mice ; Staphylococcus aureus ; Chickens ; Anti-Bacterial Agents/pharmacology ; Body Weight
مستخلص: The growing interest in employing nano-sized pharmaceutical formulations in veterinary medicine has prompted the exploration of the novel nanocarriers' ability to augment the therapeutic outcome. In this study, we harnessed niosomes, spherical nanocarriers formed through non-ionic surfactant self-assembly, to enhance the therapeutic efficacy of the broad-spectrum antibiotic florfenicol. Pre-formulation studies were conducted to identify the optimal parameters for preparing florfenicol-loaded niosomes (FLNs). These studies revealed that the formulation that consisted of Span 60, cholesterol, and dihexadecyl phosphate (DDP) at a molar ratio of 1:1:0.1 exhibited the highest entrapment efficiency (%EE) and uniform size distribution. In vitro antibacterial testing demonstrated the niosomal capacity to significantly reduce florfenicol minimum inhibitory concentration (MIC) against E. coli and S. aureus. Pharmacokinetic profiles of free florfenicol and FLN were assessed following oral administration of 30 mg florfenicol/kg body weight to healthy or E. coli-infected chickens. FLN exhibited a substantially higher maximum plasma concentration (C max ) of florfenicol compared to free florfenicol. Furthermore, FLN showed significantly higher area under the curve (AUC 0-t ) than free florfenicol as revealed from the relative bioavailability studies. Lethal dose (LD) 50 values for both free florfenicol and FLN exceeded 5 g/kg of body weight, indicating high safety profile. Assessment of mortality protection in mice against lethal E. coli infections showed the significantly higher capability of FLN to improve the survival rate (75%) than free florfenicol (25%). Collectively, these findings demonstrate the niosomal ability to improve the oral bioavailability as well as the antibacterial activity of the incorporated veterinary antibiotic florfenicol.
(© 2023. The Author(s).)
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فهرسة مساهمة: Keywords: Antibacterial activity; Antibiotics; Florfenicol; Nanoparticles; Niosome; Oral delivery
المشرفين على المادة: 0 (Liposomes)
9J97307Y1H (florfenicol)
0 (Anti-Bacterial Agents)
FLQ7571NPM (Thiamphenicol)
تواريخ الأحداث: Date Created: 20231113 Date Completed: 20240312 Latest Revision: 20240314
رمز التحديث: 20240314
مُعرف محوري في PubMed: PMC10927884
DOI: 10.1007/s13346-023-01459-9
PMID: 37957473
قاعدة البيانات: MEDLINE
الوصف
تدمد:2190-3948
DOI:10.1007/s13346-023-01459-9