Affiliation:
1. SVKM's NMIMS, Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management, Vile Parle, Mumbai, Maharashtra
400056, India
2. School of Pharmacy, GITAM (Deemed to be University), Hyderabad, Telangana 502329, India
Abstract
Controlled-release drug delivery systems (CRDDS) are more beneficial than conventional immediate
release (IRDDS) for reduced intake, prolonged duration of action, lesser adverse effects, higher bioavailability,
etc. The preparation of CRDDS is more complex than IRDDS. The hot melt extrusion (HME) technique
is used for developing amorphous solid dispersion of poorly water soluble drugs to improve their dissolution
rate and oral bioavailability. HME can be employed to develop CRDDS. Sustained release delivery systems (SRDDS),
usually given orally, can also be developed using HME. This technique has the advantages of using
no organic solvent, converting crystalline drugs to amorphous, improving bioavailability, etc. However, the
heat sensitivity of drugs, miscibility between drug-polymer, and the availability of a few polymers are some of
the challenges HME faces in developing CRDDS and SRDDS. The selection of a suitable polymer and the optimization
of the process with the help of the QbD principle are two important aspects of the successful application
of HME. In this review, strategies to prepare SRDDS and CRDDS using HME are discussed with its applications
in research.
Publisher
Bentham Science Publishers Ltd.