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PHARMACEUTICS
Year : 2011  |  Volume : 3  |  Issue : 1  |  Page : 9-14

Biodegradable chitosan-based ambroxol hydrochloride microspheres: Effect of cross-linking agents


1 SNJB's Shriman Suresh Dada Jain College of Pharmacy, Neminagar, Chandwad, Nasik, Maharastra;NANDHA College of Pharmacy, Department of Pharmaceutics, Perundurai Road, Rode, Tamil Nadu, India
2 SNJB's Shriman Suresh Dada Jain College of Pharmacy, Neminagar, Chandwad, Nasik, Maharastra, India
3 Department of Pharmaceutical Sciences, N.D.M.V.P. Samaj's, College of Pharmacy, Gangapur Road, Shivaji Nagar, Nasik - 422 002, Maharastra, India
4 NANDHA College of Pharmacy, Department of Pharmaceutics, Perundurai Road, Rode, Tamil Nadu, India

Correspondence Address:
H H Gangurde
SNJB's Shriman Suresh Dada Jain College of Pharmacy, Neminagar, Chandwad, Nasik, Maharastra;NANDHA College of Pharmacy, Department of Pharmaceutics, Perundurai Road, Rode, Tamil Nadu
India
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DOI: 10.4103/0975-1483.76414

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The objective of this study was to investigate the influence of type of cross-linking method used on the properties of ambroxol hydrochloride microspheres such as encapsulation efficiency, particle size, and drug release. Microspheres were prepared by solvent evaporation technique using chitosan as a matrix-forming agent and cross-linked using formaldehyde and heat treatment. Morphological and physicochemical properties of microspheres were then investigated by scanning electron microscopy (SEM), X-ray diffractometry (XRD), differential scanning calorimetry (DSC), and Fourier-transform infrared spectroscopy (FTIR) spectroscopy. The cross-linking of chitosan takes place at the free amino group because of formation of imine bond as evidenced by FTIR. The DSC, XRD, and FTIR analysis showed that chitosan microspheres cross linked by heating were superior in properties and performance as compared to the microspheres cross-linked using formaldehyde. SEM results revealed that heat-treated microspheres were spherical, discrete having smooth, and porous structure. The particle size and encapsulation efficiencies of the prepared chitosan microspheres ranged between 10.83-24.11 μm and 39.73-80.56%, respectively. The drug release was extended up to 12 h, and the kinetics of the drug release was obeying Higuchi kinetic proving diffusion-controlled drug release.


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