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Curcumin loaded chitosan nanoparticles impregnated into collagen-alginate scaffolds for diabetic wound healing
- Karri, Veera Venkata Satyanarayana Reddy, Kuppusamy, Gowthamarajan, Talluri, Siddhartha Venkata, Mannemala, Sai Sandeep, Kollipara, Radhakrishna, Wadhwani, Ashish Devidas, Mulukutla, Shashank, Raju, Kalidhindi Rama Satyanarayana, Malayandi, Rajkumar
- International journal of biological macromolecules 2016 v.93 pp. 1519-1529
- X-ray diffraction, amputation, antioxidants, bioavailability, biocompatibility, biodegradability, chitosan, collagen, curcumin, diabetes, differential scanning calorimetry, drug carriers, drugs, granulation tissue, inflammation, nanoparticles, particle size, pathophysiology, patients, placebos, scanning electron microscopy, solubility, tissue repair, water uptake, zeta potential
- Diabetic wounds are a common complication in patients with diabetes that often lead to amputation. Although the pathophysiology of diabetic wound is multifactorial, chronic inflammation and lack of tissue regeneration leads to impair wound healing in diabetes. Application of curcumin (CUR) which is a well-known anti-inflammatory and antioxidant agent could be better strategy in diabetic wound healing. However, low bioavailability and poor stability of CUR hinders its application. Hence, in present study a novel nanohybrid scaffold has been prepared by incorporating CUR in chitosan nanoparticles (CSNPs) to improve stability and solubility followed by impregnation of prepared CUR-CSNPs into collagen scaffold (nanohybrid scaffold) for better tissue regeneration application. The prepared CUR-CSNPs were evaluated for particle size, zeta potential, SEM, differential scanning calorimetry and X-ray powder diffraction studies and the novel nanohybrid is evaluated for morphology, biodegradability, biocompatibility, in vitro drug release and in vivo wound healing studies. The results of NPs evaluation suggest the better stability and solubility of CUR. The nanohybrid scaffold showed good in vitro characteristics in terms of better water uptake, biocompatibility and sustained drug availability. The results of in vivo wound closure analysis revealed that nanohybrid scaffold treated wounds contracted significantly (p<0.001) faster than the wounds from the control and placebo scaffold groups. Further, the obtained results suggest that complete epithelialization with thick granulation tissue formation occur in nanohybrid scaffold group, whereas lack of compact collagen deposition in placebo scaffold group and presence of inflammatory cells in control group was observed. Hence, the present study suggests that the synergistic combination of CUR (anti-inflammatory and anti-oxidant), chitosan (sustain drug carrier, wound healing) and collagen (established wound healer as scaffold) is a promising strategy to address various pathological manifestations of diabetic wounds and have better wound healing capability.