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Review
. 2013 Nov;10(11):1497-513.
doi: 10.1517/17425247.2013.821978. Epub 2013 Aug 9.

pH- and ion-sensitive polymers for drug delivery

Affiliations
Review

pH- and ion-sensitive polymers for drug delivery

Takayuki Yoshida et al. Expert Opin Drug Deliv. 2013 Nov.

Abstract

Introduction: Drug delivery systems (DDSs) are important for effective, safe, and convenient administration of drugs. pH- and ion-responsive polymers have been widely employed in DDS for site-specific drug release due to their abilities to exploit specific pH- or ion-gradients in the human body.

Areas covered: Having pH-sensitivity, cationic polymers can mask the taste of drugs and release drugs in the stomach by responding to gastric low pH. Anionic polymers responsive to intestinal high pH are used for preventing gastric degradation of drug, colon drug delivery and achieving high bioavailability of weak basic drugs. Tumor-targeted DDSs have been developed based on polymers with imidazole groups or poly(β-amino ester) responsive to tumoral low pH. Polymers with pH-sensitive chemical linkages, such as hydrazone, acetal, ortho ester and vinyl ester, pH-sensitive cell-penetrating peptides and cationic polymers undergoing pH-dependent protonation have been studied to utilize the pH gradient along the endocytic pathway for intracellular drug delivery. As ion-sensitive polymers, ion-exchange resins are frequently used for taste-masking, counterion-responsive drug release and sustained drug release. Polymers responding to ions in the saliva and gastrointestinal fluids are also used for controlled drug release in oral drug formulations.

Expert opinion: Stimuli-responsive DDSs are important for achieving site-specific and controlled drug release; however, intraindividual, interindividual and intercellular variations of pH should be considered when designing DDSs or drug products. Combination of polymers and other components, and deeper understanding of human physiology are important for development of pH- and ion-sensitive polymeric DDS products for patients.

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Figures

Figure 1
Figure 1. Representative drug delivery systems with stimulus-responsive capability
A. Polymeric mixed micelles prepared with poly(l-lactic acid)-block-poly(ethylene glycol)-block-poly(His)-TAT peptide and poly(His)-block-poly(ethylene glycol) for exposure of TAT cell-penetrating peptides responsive to the tumoral acidic pH [50]. B. A bead system containing drug and organic acid in the core and coated with a Eudragit RS layer for ion-sensitive sigmoidal drug release [100,101]. C. Tablets containing drug and Na2SO4 and coated with a PNIPAM layer for ion-sensitive colon drug delivery [108]. D. ‘Salting-out taste-masking systems’ consisting of a drug core, a salting-out layer containing salts and water-soluble polymers, and a water-penetration-control layer of water-insoluble materials for ion-sensitive taste-masking of oral disintegrating tablets [16-19].
Figure 2
Figure 2. Drug release from ion-exchange resins
A. Drug release from the resins is governed by an equilibrium exchange reaction. B. During storage, the drug-resin complexes can be maintained in liquid free of the counterions of resins. After oral administration, drug release is promoted by the ions present in the saliva and gastrointestinal fluids. Secretion of the saliva and gastrointestinal fluids and absorption of the released drug promote the drug release.

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