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Enhanced efficacy of clindamycin hydrochloride encapsulated in PLA/PLGA based nanoparticle system for oral delivery.
Rauta, Pradipta Ranjan; Das, Niladri Mohan; Nayak, Debasis; Ashe, Sarbani; Nayak, Bismita.
Afiliación
  • Rauta PR; Immunology and Molecular Medicine Lab, Department of Life Science, National Institute of Technology Rourkela, Odisha 769008, India.
  • Das NM; Immunology and Molecular Medicine Lab, Department of Life Science, National Institute of Technology Rourkela, Odisha 769008, India.
  • Nayak D; Immunology and Molecular Medicine Lab, Department of Life Science, National Institute of Technology Rourkela, Odisha 769008, India.
  • Ashe S; Immunology and Molecular Medicine Lab, Department of Life Science, National Institute of Technology Rourkela, Odisha 769008, India.
  • Nayak B; Immunology and Molecular Medicine Lab, Department of Life Science, National Institute of Technology Rourkela, Odisha 769008, India. nayakb@nitrkl.ac.in.
IET Nanobiotechnol ; 10(4): 254-61, 2016 Aug.
Article en En | MEDLINE | ID: mdl-27463797
Clindamycin hydrochloride (CLH) is a clinically important oral antibiotic with wide spectrum of antimicrobial activity that includes gram-positive aerobes (staphylococci, streptococci etc.), most anaerobic bacteria, Chlamydia and certain protozoa. The current study was focused to develop a stabilised clindamycin encapsulated poly lactic acid (PLA)/poly (D,L-lactide-co-glycolide) (PLGA) nano-formulation with better drug bioavailability at molecular level. Various nanoparticle (NPs) formulations of PLA and PLGA loaded with CLH were prepared by solvent evaporation method varying drug: polymer concentration (1:20, 1:10 and 1:5) and characterised (size, encapsulation efficiency, drug loading, scanning electron microscope, differential scanning calorimetry [DSC] and Fourier transform infrared [FTIR] studies). The ratio 1:10 was found to be optimal for a monodispersed and stable nano formulation for both the polymers. NP formulations demonstrated a significant controlled release profile extended up to 144 h (both CLH-PLA and CLH-PLGA). The thermal behaviour (DSC) studies confirmed the molecular dispersion of the drug within the system. The FTIR studies revealed the intactness as well as unaltered structure of drug. The CLH-PLA NPs showed enhanced antimicrobial activity against two pathogenic bacteria Streptococcus faecalis and Bacillus cereus. The results notably suggest that encapsulation of CLH into PLA/PLGA significantly increases the bioavailability of the drug and due to this enhanced drug activity; it can be widely applied for number of therapies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácido Poliglicólico / Clindamicina / Fenómenos Fisiológicos Bacterianos / Ácido Láctico / Preparaciones de Acción Retardada / Nanocápsulas Idioma: En Revista: IET Nanobiotechnol Asunto de la revista: BIOTECNOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácido Poliglicólico / Clindamicina / Fenómenos Fisiológicos Bacterianos / Ácido Láctico / Preparaciones de Acción Retardada / Nanocápsulas Idioma: En Revista: IET Nanobiotechnol Asunto de la revista: BIOTECNOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: India
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