Nanostructure-coated diclofenac-loaded microparticles:: Preparation, morphological characterization, in vitro release and in vivo gastrointestinal tolerance

被引:32
作者
Beck, RCR
Pohlmann, AR
Benvenutti, EV
Costa, TD
Guterres, SS
机构
[1] Univ Fed Rio Grande Sul, Fac Farm, Programa Posgrad Ciencias Farmaceut, BR-90610000 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande Sul, Inst Quim, Dept Quim Organ, BR-91501970 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande Sul, Inst Quim, Dept Quim Inorgan, BR-91501970 Porto Alegre, RS, Brazil
关键词
diclofenac; polymer; nanostructure-coating; microparticles; gastrointestinal tolerance;
D O I
10.1590/S0103-50532005000700022
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work reports the preparation and characterization of polymeric nanostructure-coated diclofenac-loaded microparticles. After spray-drying, powders presented 80% of yield and encapsulation efficiency of 83%. SEM analyses showed nanostructures adsorbed onto the surface of microparticles presenting surface area (BET) and pore volumes (BJH) (83 m(2) g(-1), 0.10 cm(3) g(-1)) smaller than the uncoated-core (163 m(2) g(-1), 0.25 cm(3) g(-1)). In vitro drug release experiments at pH 5.0 and 7.4 showed dissolution efficiencies of 34% and 78% (uncoated-core), 74% and 83% (physical mixture of raw materials), and 58% and 85% (nanostructure- coated microparticles), respectively. Mathematical modeling of the dissolution profiles fitted a biexponential model at pH 5.0 and a monoexponential model at pH 7.4. Regarding the digestive tolerance experiments, the total lesional indexes were 156.1 +/- 48.5 for sodium diclofenac aqueous solution, 132.4 +/- 45.7 for uncoated-core, 109.1 +/- 35.8 for physical mixture and 29.9 +/- 12.1 for microparticles showing a protective effect of these microparticles against the mucosal diclofenac damage. This strategy of coating presents a potential use for oral administration of drugs.
引用
收藏
页码:1233 / 1240
页数:8
相关论文
共 42 条
[1]  
AMMOURY N, 1993, CLIN MATER, V13, P121, DOI 10.1016/0267-6605(93)90098-R
[2]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[3]   Nanoparticle-coated microparticles: preparation and characterization [J].
Beck, RCR ;
Pohlmann, AR ;
Guterres, SS .
JOURNAL OF MICROENCAPSULATION, 2004, 21 (05) :499-512
[4]   PREPARATION OF BIODEGRADABLE POLY (+/-) LACTIDE MICROPARTICLES USING A SPRAY-DRYING TECHNIQUE [J].
BODMEIER, R ;
CHEN, HG .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1988, 40 (11) :754-757
[5]   RECENT ADVANCES ON THE USE OF BIODEGRADABLE MICROPARTICLES AND NANOPARTICLES IN CONTROLLED DRUG-DELIVERY [J].
BRANNONPEPPAS, L .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 116 (01) :1-9
[6]   THE SPRAY DRYING OF PHARMACEUTICALS [J].
BROADHEAD, J ;
ROUAN, SKE ;
RHODES, CT .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1992, 18 (11-12) :1169-1206
[7]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[8]   Comparative in vitro evaluation of several colloidal systems, nanoparticles, nanocapsules, and nanoemulsions, as ocular drug carriers [J].
Calvo, P ;
VilaJato, JL ;
Alonso, MJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (05) :530-536
[9]   PH-SOLUBILITY RELATIONSHIP AND PARTITION-COEFFICIENTS FOR SOME ANTI-INFLAMMATORY ARYLALIPHATIC ACIDS [J].
CHIARINI, A ;
TARTARINI, A ;
FINI, A .
ARCHIV DER PHARMAZIE, 1984, 317 (03) :268-273
[10]   SPRAY-DRIED POLYLACTIDE MICROSPHERE PREPARATION - INFLUENCE OF THE TECHNOLOGICAL PARAMETERS [J].
CONTE, U ;
CONTI, B ;
GIUNCHEDI, P ;
MAGGI, L .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1994, 20 (03) :235-258