Preparation of Drug Eluting Natural Composite Scaffold Using Response Surface Methodology and Artificial Neural Network Approach.
10.1007/s13770-017-0100-z
- Author:
Shailendra Singh SHERA
1
;
Shraddha SAHU
;
Rathindra Mohan BANIK
Author Information
1. Bioprocess Technology Laboratory, School of Biochemical Engineering, Indian Institute of Technology (Banaras Hindu University), Varanasi, Lanka, Varanasi, Uttar Pradesh 221005, India. rmbanik@gmail.com
- Publication Type:Original Article
- Keywords:
Artificial neural network;
Response surface methodology;
Controlled drug delivery;
Silk fibroin/xanthan
- MeSH:
Chloramphenicol;
Diffusion;
Drug Liberation;
Fibroins;
Gram-Negative Bacteria;
Porosity;
Silk;
Tissue Engineering
- From:
Tissue Engineering and Regenerative Medicine
2018;15(2):131-143
- CountryRepublic of Korea
- Language:English
-
Abstract:
Silk fibroin/xanthan composite was investigated as a suitable biomedical material for controlled drug delivery, and blending ratios of silk fibroin and xanthan were optimized by response surface methodology (RSM) and artificial neural network (ANN) approach. A non-linear ANN model was developed to predict the effect of blending ratios, percentage swelling and porosity of composite material on cumulative percentage release. The efficiency of RSM was assessed against ANN and it was found that ANN is better in optimizing and modeling studies for the fabrication of the composite material. In-vitro release studies of the loaded drug chloramphenicol showed that the optimum composite scaffold was able to minimize burst release of drug and was followed by controlled release for 5 days. Mechanistic study of release revealed that the drug release process is diffusion controlled. Moreover, during tissue engineering application, investigation of release pattern of incorporated bioactive agent is beneficial to predict, control and monitor cellular response of growing tissues. This work also presented a novel insight into usage of various drug release model to predict material properties. Based on the goodness of fit of the model, Korsmeyer–Peppas was found to agree well with experimental drug release profile, which indicated that the fabricated material has swellable nature. The chloramphenicol (CHL) loaded scaffold showed better efficacy against gram positive and gram negative bacteria. CHL loaded SFX55 (50:50) scaffold shows promising biocomposite for drug delivery and tissue engineering applications.
