The
objective of this study is to fabricate biodegradable polymers
into scaffolds to embed drugs for tumor treatment without any toxic
side effects. Scaffold preparation is optimized by changing the conditions,
e.g., poly(lactic acid) concentration (10% w/v), applied potential
(15 kV), flow rate (1 mL/h), distance between needle and collector
(20 cm), and nanosheet concentration (4 wt % nanoclay), during electrospinning.
A drug-embedded nanofiber scaffold is used to regulate the drug delivery
in a sustainable manner utilizing the enhanced barrier effect from
dispersed nanosheet and good interaction between the components. The
effect of thermal treatment improves the stability and slower release
of drug through alteration in microstructure. Cell culture studies
using a nanofiber scaffold indicate its biocompatibility and applicability
as a biomaterial for tumor treatment. Sustained drug release from
the scaffold enhances the in vitro cancer cytotoxicity
up to 85% in 3 days. In vivo studies clearly suggest
suppression of tumor volume using scaffold as a patch over the tumor
site as compared to control, pure drug, and drug-embedded film in
the mice model. Evaluation of biochemical parameters indicates no
toxic side effects for the liver and kidney using a hybrid scaffold
as a delivery vehicle as opposed to severe liver injury in control
and pure drug-treated mice group. Histopathology of the organs confirms
the side effects for the pure drug-treated mice group against normal
tissue morphology observed in scaffold-treated animals. Thus, sustained
release of drug from this novel delivery vehicle has every potential
to be used for tumor treatment more efficiently without any considerable
side effects.