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ABSTRACT Hybrid membranes based on poly(vinyl alcohol) (PVA) of widely different molecular weights and ex situ nanosilica were synthesized and characterized as transdermal delivery device for Diltiazem hydrochloride. Investigations showed that change in PVA molecular weight strongly influenced physico-mechanicals of the hybrids especially at low nanosilica content than at higher levels. As for example at 1 wt %, low molecular weight PVA induced finer dispersion of silica nanoparticles resulting into higher dry state crystallinity and mechanical strength but slightly lower biocompatibility as compared to high molecular weight PVA. Those variations in physico-mechanicals finally affected Diltiazem retention and its elution from those membranes under physiological conditions. Low molecular weight PVA produced highest drug retention as well as slowest yet steady release than both high molecular weight PVA and neat PVA membranes. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2076-2086, 2013 [ABSTRACT FROM AUTHOR]

Abstract: This paper reports interesting differences between physical and mechanical properties of various membranes prepared from high and low molecular weight poly (vinyl alcohol) (PVA) and xanthan gum (XG) blends irradiated under low dose electron beam. The membranes were designed for sustained delivery of diltiazem hydrochloride through skin. Electron beam irradiation produced crosslinks and turned PVA into crystalline phase from its amorphous organization in the unirradiated state. PVA crystals were fibrillar at low XG content (1wt.%) when the molecular weight was high while similar orientation at higher XG content (5wt.%) when the molecular weight was low. Low molecular weight PVA–XG membranes showed equivalent physical properties under dry condition but wet-mechanical properties were superior for high molecular weight PVA–XG hybrids. Both of them showed slow and sustained diltiazem release but the later induced slightly slower release despite low drug encapsulation efficiency due to its better wet mechanical strength. [Copyright &y& Elsevier]

Interesting correlation between physicomechanical and in vitro release behavior of diltiazem hydrochloride has been obtained in physically treated poly(vinyl alcohol) (PVA) membranes of widely different molecular weights. Physical treatment could not raise crystallinity in dry state, but some of them show significant postswelled crystallinity and achieves elastomeric character. They also retain lot of equilibrium water, ideally suited for drug-impregnated transdermal patches. In effect, low molecular weight PVA and dimethyl sulfoxide-modified high molecular weight PVA membranes have shown acceptable release of diltiazem hydrochloride when compared with thermally treated high molecular weight PVA membrane. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 [ABSTRACT FROM AUTHOR]

Abstract: Extremely fast release of diltiazem hydrochloride (water soluble, anti anginal drug used to treat chest pain) together with its faster erosion has been the primary problem in conventional oral therapy. It has been addressed in this paper by encapsulating the drug in electron beam irradiated various poly (vinyl alcohol) hydrogel membranes and delivering it through transdermal route. Results show excellent control over the release of diltiazem hydrochloride through these membranes subject to their physico-mechanicals. [Copyright &y& Elsevier]

Aqueous nanosilica sol (particle size range: 9-13 nm, pH: 9.0) was added at various low concentration range (0.5-2 wt.%) into aqueous poly (vinyl alcohol) (PVA) of different molecular weight (98% hydrolyzed, 20 wt.%) (pH: 5.0) at room temperature under constant stirring to synthesize organic-inorganic hybrid hydrogels in presence of sodium lauryl sulphate as a silica dispersant. Buffer tablets were added to arrest the pH at 9.0 (to prevent any silica aggregation due to change in pH). The resultant hybrids were cast on Teflon sheets and dried in an oven at 50°C to drive out all the unbound water. Those films were then subjected to freese-thaw treatment continuously for 5 h. The freese-thawed films appeared opaque. The swelling-de swelling experiments with the hydrogels were carried out in distilled water at room temperature and consequently allowed to de-swell naturally. Those observations were correlated with the microstructures of the hybrid hydrogels. [ABSTRACT FROM AUTHOR]