Microspheres containing Doxycycline: Properties and in vitro study

Authors

  • Rima Kassab
  • Paolo Yammine Department of Chemistry, Faculty of Sciences, University of Balamand, Tripoli, Lebanon
  • Dima Moussa Department of Chemistry, Faculty of Sciences, University of Balamand, Tripoli, Lebanon
  • Nahed Safi Department of Chemistry, Faculty of Sciences, University of Balamand, Tripoli, Lebanon

Keywords:

Poly(DL-lactide), doxycycline, microspheres, solvent evaporation technique, drug release

Abstract

PLA microspheres loaded with the antibiotic Doxycycline are prepared using solvent evaporation technique (o/w) by varying the drug masses. They are evaluated for drug encapsulation, drug loading, particle size, morphology, FT-IR, stability and in vitro release. Microspheres loaded with Doxycycline show a maximum drug encapsulation of 38%. They exhibit homogeneous size distribution varying between 80 and 110 øm, with a spherical profile and porous surface. FT-IR study hasnÊt revealed any drug-polymer interaction. After 6 months of storage at different conditions, no appreciable difference is observed concerning the degradation of microspheres. In vitro release study of PLA microspheres loaded with Doxycycline reveals a rather fast release which requires only few hours to go to completion.

References

. Narasimha RR, Sampath KM, Dileep KK,

Vineeth P. Formulation and evaluation of

capcitabine microspheres. Int J Pharm

Tech. 2001;3(2):2599-2632.

. Nidhi G: Development and

characterization of dental films containing

Tetracycline HCl for periodontitis.

MasterÊs thesis. University of Georgia,

Athens; 2004

. Sun Y, Peng Y, Chen Y, Shukla AJ.

Application of artificial neural networks in

the design of controlled release drug

delivery systems. Adv Drug Deliv Rev.

;55(9):1201ă1215.

. Hanwei Z, Jianzhong B, Shenguo W.

Preparation and drug release behaviors

of 5-Fluorouracil Loaded poly(glycolideco-lactide-co-caprolactone) nanoparticles.

J Appl Polymer Sci. 2007;106(6):3757-

. Heidi MM, Sohn MJ, Al-Ghananeem A,

DeLuca PP. Materials for Pharmaceutical

Dosage Forms: Molecular pharmaceutics

and controlled release drug delivery

aspects. Int J mol sci. 2010;11(9):3298-

. Sadeghi M. Pectin-based biodegradable

hydrogels with potential biomedical

applications as drug delivery systems. J

Biomater Nanobiotechnol. 2011;2(1):36-

. Giavaresi G, Tschon M, Borsari V, Daly

JH, Liggat JJ, Fini M, Bonazzi V, Nicolini

A, Carpi A, Morra M, Cassinelli C,

Giardino R. New polymers for drug

delivery systems in orthopaedics: in vivo

biocompatibility evaluation. Biomed

Pharmacother. 2004;58(8):411ă417

. Seyednejad H, Ghassemi AH, Van

Nostrum CF, Vermonden T, Hennink WE.

Functional aliphatic polyesters for

biomedical and pharmaceutical

applications. J Contr Release.

;152(1):168-176

. Letizia MM: Chitosan and plga

microspheres as drug delivery system

against pulmonary mycobacteria

infections. PhD thesis. University of

Cagliari, Department Farmaco Chimico

Tecnologico, Italy; 2009

. Perrin DE, English JP. Polyglycolide and

polylactide. In: Domb AJ, Kost J,

Wiseman DW, editors. Handbook of

Biodegradable Polymers. Harwood

Academic Publishers, Amsterdam; 1997.

p.1ă27

. Ruan G, Feng SS. Preparation and

characterization of poly(lactic acid)ă

poly(ethylene glycol)ăpoly(lactic acid)

(PLAăPEGăPLA) microspheres for

controlled release of paclitaxel.

Biomaterials. 2003;24(27):5037-5044

. Suong-Hyu H. Biodegradable poly(lactic

acid) microspheres for drug delivery

systems. Yonsei Med J. 2000;14(6):720-

. Shenoy DB, DÊSouza, RJ, Udupa N.

Poly(DL-lactide-co-glycolide) microporous

microsphere-based depot formulation of a

peptide-like anti-neoplastic agent. J

Microencapsul. 2002;19(4):523ă535

. Dinarvand R, Moghadam SH,

Mohammadyari-Fard L, Atyabi F.

Preparation of biodegradable

microspheres and matrix devices

containing Naltrexone. AAPS

ParmSciTech. 2003;4(3):45-54

. Fernandez-Carballido A, Herrero-Vanrell

R, Molina-Martinez IT, Pastoriza P.

Sterilized ibuprofen-loaded poly (D,Llactide-co-glycolide) microspheres for

intra-articular administration: effect of

gamma-irradiation and storage. J

Microencapsul. 2004;21(6):653ă665

. La SB, Okano T, Kataoka K. Preparation

and characterization of the micelleforming polymeric drug indomethacinincorporated poly(ethylene oxide)-

poly(beta-benzyl L-aspartate) block

copolymer micelles. J Pharmaceut Sci.

;85(1):85ă90

. Giovagnoli S, Tsai T, DeLuca PP.

Formulation and release behavior of

doxycycline-alginate hydrogel

microparticles embedded into pluronic

F127 thermogels as a potential new

vehicle for Doxycycline intradermal

sustained delivery. AAPS PharmSciTech.

;11(1):212ă220

. Standiford HC: Tetracyclines and

chloramphenicol. In: Mandell GL, Douglas

RG, Bennett JE, editors. Principles and

practice of infectious diseases. Churchill

Livingstone, Inc., New York; 1990. p.284-

. Aurer A, Plancak D. Antimicrobial

treatment of periodontal diseases. Acta

Stomatol Croat. 2004;38(1):67-72

. Yoon Y, Kinam P. Control of

Encapsulation Efficiency and Initial Burst

in Polymeric Microparticle Systems. Arch

of pharm Res. 2004;27(1):1-12

. Mehta RC, Thanoo BC, DeLuca PP.

Peptide containing microspheres from low

molecular weight and hydrophilic

poly(D,L-lactide-co-glycolide). J Contr

Release. 1996;41(3):249- 257

. Chung TW, Huang YY, Liu YZ. Effect of

the rate of solvent evaporation on the

characteristics of drug loaded PLLA and

PDLA microspheres. Int J Pharm.

;212(2):161-169

. Okada H, Toguchi H. Biodegradable

microspheres in drug delivery. Crit Rev

Ther Drug Carrier Syst. 1995;12(1):1-99

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Published

2013-09-30

How to Cite

Rima Kassab, Paolo Yammine, Dima Moussa, & Nahed Safi. (2013). Microspheres containing Doxycycline: Properties and in vitro study. International Journal of Drug Delivery, 5(3), 264–269. Retrieved from https://ijdd.arjournals.org/index.php/ijdd/article/view/205

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Original Research Articles