Abstract

Thin films were prepared using layer-by-layer (LbL) deposition of Nafion (NAF) and polycations such as poly(allylamine hydrochloride) (PAH), poly(ethyleneimine) (PEI), and poly(diallydimethylammonium chloride) (PDDA). Insulin was then adsorbed on the NAF-polycation LbL films by immersion in an insulin solution. The NAF-polycation LbL films were characterized using a quartz crystal microbalance and an atomic force microscope. The release of insulin from the LbL films was characterized using UV-visible adsorption spectroscopy and fluorescence emission spectroscopy. The greatest amount of insulin was adsorbed on the NAF-PAH LbL film. The amount of insulin adsorbed on the (NAF/PAH)5NAF LbL films by immersion in a 1 mg mL−1 insulin solution at pH 7.4 was 61.8 µg cm−2. The amount of insulin released from the LbL films was higher when immersed in insulin solutions at pH 2.0 and pH 9.0 than at pH 7.4. Therefore, NAF-polycations could be employed as insulin delivery LbL films under mild conditions and as an insulin release control system according to pH change.

Highlights

  • Layer-by-layer (LbL) films can be prepared by alternate and repeated deposition of a polyelectrolyte on a solid surface through electrostatic interactions [1,2]

  • The value of −∆F was increased when the quartz resonator was exposed to NAF and poly(allylamine hydrochloride) (PAH), PEI, or poly(diallydimethylammonium chloride) (PDDA), which indicated that NAF-PAH, NAF-PEI, and NAF-PDDA

  • It is considered that negatively charged NAF and positively charged PAH, PEI, and PDDA are deposited by electrostatic attraction, which builds up the LbL film on the quartz resonator surface

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Summary

Introduction

Layer-by-layer (LbL) films can be prepared by alternate and repeated deposition of a polyelectrolyte on a solid surface through electrostatic interactions [1,2]. The materials employed for this purpose include synthetic polymers [8,9,10], proteins [11], polysaccharides [12,13], and DNA [14]. Such layered thin films have found applications in separation and purification [15,16], sensors [17,18,19], microcapsules [20,21], and drug delivery systems (DDSs) [22,23]. LbL based DDS that responds to pH [24,25,26] and sugar levels [27,28,29,30].

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