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Polyelectrolyte complexes of gum kondagogu and chitosan, as diclofenac carriers
被引:83
|作者:
Naidu, V. G. M.
[1
]
Madhusudhana, K.
[1
]
Sashidhar, R. B.
[3
]
Ramakrishna, S.
[1
]
Khar, Roop K.
[4
]
Ahmed, Farhan J.
[4
]
Diwan, Prakash V.
[1
,2
]
机构:
[1] Indian Inst Chem Technol, Div Pharmacol, Hyderabad 500007, Andhra Pradesh, India
[2] Natl Inst Pharmaceut & Educ Res, Hyderabad, Andhra Pradesh, India
[3] Osmania Univ, Univ Coll Sci, Dept Biochem, Hyderabad 500007, Andhra Pradesh, India
[4] Jamia Hamdard Deemed Univ, Dept Pharmaceut, Fac Pharm, New Delhi, India
关键词:
Polyelectrolyte complex;
Gum kondagogu;
Chitosan;
Diclofenac sodium;
Controlled delivery;
Bioavailability;
Anti-inflammatory;
COCHLOSPERMUM-GOSSYPIUM;
CHONDROITIN SULFATE;
POLY(ACRYLIC ACID);
SODIUM ALGINATE;
PH-SENSITIVITY;
CROSS-LINKING;
RELEASE;
MICROSPHERES;
DELIVERY;
PECTIN;
D O I:
10.1016/j.carbpol.2008.11.010
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Polyelectrolyte complexes (PEC) of gum kondagogu (GKG) and chitosan were prepared by mixing polymeric solutions of different concentrations (0.02-0.18% w/v). The complex formed were loaded with diclofenac sodium, and the release of the drug was measured in vitro and in vivo, along with the measurement of particle size, zeta potential, complex formation, flow properties, and loading efficiency. Maximum yield of PEC was observed at gum kondagogu concentrations above 80%. The PEC showed lower release of diclofenac sodium in 0.1 N HCl as compared to phosphate buffer (pH 6.8). Increasing the concentration of gum kondagogu in PEC led to an increase in drug release. However, PEC 1:3 (gum kondagogu: chitosan) with higher concentration of chitosan showed 98% release with in 4.5 h, owing to the fact that chitosan has a higher degree of swelling in acidic medium. PEC 5:1 and 3:1 showed a 5.3- and 5.8-fold increase in relative bioavailability compared to the free drug when administered orally to the rats. (C) 2009 Published by Elsevier Ltd.
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页码:464 / 471
页数:8
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