Literature DB >> 9685895

Transdermal iontophoresis: modulation of electroosmosis by polypeptide.

J Hirvonen1, R H Guy.   

Abstract

The objective of this research was to further evaluate the relative importance of electrorepulsion and electroosmosis to the mechanism of enhanced transport across the skin during iontophoresis. Specifically, the impact of iontophoresing into the skin positively and negatively charged polypeptides (poly-L-lysines and poly-L-glutamic acids, respectively) on the membrane's permselectivity and hence on the quantity and direction of electroosmotic flow, was examined. Experiments were performed in vitro at pH 7.4 using conventional methodology; electroosmosis during the iontophoresis of the polypeptides into and across the skin was tracked in the usual way via the movement of the polar, uncharged, non-metabolizable marker, D-mannitol. Electrotransport of the cationic polypeptides attenuated electroosmotic flow in the normal anode-to-cathode direction; the degree of inhibition was correlated both with the initial concentration of poly-L-lysine in the anodal chamber and with the molecular weight of the polypeptide employed (from 1 to 25 kilodaltons). Iontophoresis of the anionic poly-L-glutamic acids from the cathode provoked a slight increase in electroosmotic flow in the 'reverse' direction (i.e. from the receptor phase beneath the skin towards the cathode chamber located on the epidermal side of the membrane); this effect, however, was much less dramatic than that produced in the opposite sense by the cationic polypeptides. The results suggest that driving large positively-charged polypeptide molecules into the skin leads to neutralization of the membrane's negativity, a subsequent loss of permselectivity and a concomitant attenuation of electroosmosis in the conventional anode-to-cathode direction. Presumably, the relatively poor iontophoretic permeability of these species (which becomes more and more evident with increasing molecular weight) results in a sufficiently important association of the polypeptide with the skin during the period of current passage. Much less significant effects are realized by the cathodal iontophoresis of poly-anions due to the difficulty of 'pushing' negative ions into an already negatively-charged membrane.

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Year:  1998        PMID: 9685895     DOI: 10.1016/s0168-3659(97)00150-8

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  6 in total

1.  Structure-skin permeability relationship of dendrimers.

Authors:  Venkata Vamsi Venuganti; Preety Sahdev; Michael Hildreth; Xiangming Guan; Omathanu Perumal
Journal:  Pharm Res       Date:  2011-06-02       Impact factor: 4.200

2.  Transdermal iontophoretic delivery of vapreotide acetate across porcine skin in vitro.

Authors:  Yannic B Schuetz; Aarti Naik; Richard H Guy; Evelyne Vuaridel; Yogeshvar N Kalia
Journal:  Pharm Res       Date:  2005-08-03       Impact factor: 4.200

3.  Contributions of electromigration and electroosmosis to iontophoretic drug delivery.

Authors:  D Marro; Y N Kalia; M B Delgado-Charro; R H Guy
Journal:  Pharm Res       Date:  2001-12       Impact factor: 4.200

4.  Transdermal delivery of cytochrome C--A 12.4 kDa protein--across intact skin by constant-current iontophoresis.

Authors:  J Cázares-Delgadillo; A Naik; A Ganem-Rondero; D Quintanar-Guerrero; Y N Kalia
Journal:  Pharm Res       Date:  2007-04-25       Impact factor: 4.200

5.  Modulation of Electroosmotic Flow through Skin: Effect of Poly(Amidoamine) Dendrimers.

Authors:  Hye Ji Kim; Seaung Youl Oh
Journal:  Biomol Ther (Seoul)       Date:  2018-03-01       Impact factor: 4.634

6.  Specific protein-protein interactions limit the cutaneous iontophoretic transport of interferon beta-1B and a poly-ARG interferon beta-1B analogue.

Authors:  S Dubey; R Perozzo; L Scapozza; Y N Kalia
Journal:  Int J Pharm X       Date:  2020-07-08
  6 in total

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