Sentence examples for controlled release delivery from inspiring English sources

It is very important to enhance the absorption simultaneously while designing controlled release delivery systems for poorly water-soluble and poorly permeable drugs (BCS IV).

These studies demonstrate that the designed compression-coated tablets may be a promising strategy for peroral controlled release delivery system of water-insoluble drugs.

Therefore, some lab successfully solved the problem by developing the smart and innovative drug delivery systems in biomedical applications (such as superparamagnetic multistage delivery system [14], supramolecular microcapsules controlled release delivery system [15]).

In designing sustained or controlled release delivery systems of herbal medicines, we developed the concept of synchronized release which was characterized by keeping active components' initial ratio throughout the whole release process.

In this study, starch-based microparticles (MPs) fabricated by a water-in-water (w/w) emulsification-crosslinking method could be used as a controlled release delivery vehicle for food bioactives.

In another study, the effects of AIDD on hydromorphone hydrochloride formulated using OROS Push-Pull, a well known osmotically controlled release delivery system, was investigated in healthy subjects under fed and fasted conditions in an open-label, randomized, four-treatment, four-period, four-sequence, crossover study (Sathyan et al. 2008).

The purpose of this chapter is to provide a perspective on controlled release drug delivery systems for companion animals and highlight some of the reasons why controlled release drug delivery systems are developed for companion animals.

Controlled release drug delivery systems offer great advantages over the conventional dosage forms.

Polymeric nanoparticles reached this status due to biocompatibility, non-toxicity to biological systems, biodegradability, stability during storage, controlled release, target delivery, resulting in higher therapeutic efficacy [21, 25, 28, 29].

PLGA microspheres are widely studied for controlled release drug delivery applications, and many models have been proposed to describe PLGA degradation and erosion and drug release from the bulk polymer.

First, the limitations of cytokine-based therapy are mostly due to tissue transport, pharmacokinetics and protein stability, and this reinforces the need to develop controlled release and delivery strategies for the SCS.