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Radiolytic synthesis provides a convenient and environmentally-friendly approach to prepare metallic nanoparticles in large scale with narrow size distribution. In this report, colloidal silver nanoparticles (AgNPs) were synthesized by gamma radiation using poly(vinyl alcohol) (PVA) or silk fibroin (SF) as stabilizers and were evaluated for their antibacterial properties. The conversion of metallic silver ions to silver atoms depended on irradiation dose and stabilizer concentration as determined by UV-Vis spectrophotometry and transmission electron microscopy. The uniformly dispersed AgNPs with diameter 32.3 ± 4.40 nm were evaluated as antiseptic agents in films composed of chitosan, SF, and PVA that were processed by irradiation-induced crosslinking. Using disc diffusion assay, the films containing 432 ppm AgNPs could effectively inhibit the growth of bothStaphylococcus aureusandPseudomonas aeruginosa. Therefore, we have demonstrated in our present study that gamma radiation technique can potentially be applied in the mass production of antibacterial wound dressings.

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Introduction Functionalization of water-soluble chitosan (WSCS) nanocolloids with, gold nanoparticles (AuNPs), and LyslLys3 (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid)-bombesin 1–14 (DOTA-BBN) peptide affords an innovative pathway to produce prostate tumor cell-specific nanomedicine agents with potential applications in molecular imaging and therapy. Methods The preparation involves the production and full characterization of water-soluble chitosan (WSCS), via gamma (γ) rays (80 kGy) irradiation, followed by DOTA-BBN conjugation for subsequent use as an effective template toward the synthesis of tumor cell-specific AuNPs-WSCS-DOTA-BBN. Results The WSCS-DOTA-BBN polymeric nanoparticles (86 ± 2.03 nm) served multiple roles as reducing and stabilizing agents in the overall template synthesis of tumor cell-targeted AuNPs. The AuNPs capped with WSCS and WSCS-DOTA-BBN exhibited average Au-core diameter of 17 ± 8 nm and 20 ± 7 nm with hydrodynamic diameters of 56 ± 1 and 67± 2 nm, respectively. The AuNPs-WSCS-DOTA-BBN showed optimum in vitro stability in biologically relevant solutions. The targeted AuNPs showed selective affinity toward GRP receptors overexpressed in prostate cancer cells (PC-3 and LNCaP). Discussion The AuNPs-WSCS-DOTA-BBN displayed cytotoxicity effects against PC-3 and LNCaP cancer cells, with concomitant safety toward the HAECs normal cells. The AuNPs-WSCS-DOTA-BBN showed synergistic targeting toward tumor cells with selective cytotoxicity of AuNPs towards PC-3 and LNCaP cells. Our investigations provide compelling evidence that AuNPs functionalized with WSCS-DOTA-BBN is an innovative nanomedicine approach for use in molecular imaging and therapy of GRP receptor-positive tumors. The template synthesis of AuNPs-WSCS-DOTA-BBN serves as an excellent non-radioactive surrogate for the development of the corresponding 198 AuNPs theragnostic nanoradiopharmaceutical for use in cancer diagnosis and therapy.

This research aimed to scale up the production of starch-based super water absorbent (SWA) and to validate the practical benefits of SWA for agricultural applications. SWA was successfully prepared in an up-scaling production by radiation-induced graft polymerization of acrylic acid onto cassava starch. Chemical characterization by FTIR and thermal characterization by TGA showed results that differentiated starting materials from the prepared SWA, thus confirming effective preparation of starch-based SWA via radiation-induced graft polymerization. SEM results visibly revealed a highly porous morphology of the synthesized SWA, substantiating its high swelling ability. Results from the field tests, performed for two seasons, revealed that the prepared SWA was able to increase the survival rate of young rubber trees planted in arid area by up to 40%, while simultaneously enhancing the growth characteristics of the young rubber trees.

Purpose:We report herein bombesin peptide conjugated water-soluble chitosan gallate as a template for rapid one-pot synthesis of gold nanoparticles (AuNPs) with capabilities to target receptors on prostate cancer cells. Methods: Water-soluble chitosan (WCS), anchored with gallic acid (GA) and LyslLys3 (1,4,7,10-tetraazacyclo dodecane-1,4,7,10-tetraacetic acid) bombesin 1-14 (DBBN) peptide, provides a tumor targeting nanomedicine agent. WCS nanoplatforms provide attractive strategies with built-in capabilities to reduce gold (III) to gold nanoparticles with stabilizing and tumor-targeting capabilities. WCS-GA-DBBN encapsulation around gold nanoparticles affords optimum in vitro stability. Results:The DBBN content in the WCS-GA-DBBN sample was ~27%w/w. The antioxidant activities of WCS-GA and WCS-GA-DBBN nanocolloids were enhanced by 12 times as compared to the nascent WCS. AuNPs with a desirable hydrodynamic diameter range of 40-60 nm have been efficiently synthesized using WCS-GA and WCS-GA-DBBN platforms. The AuNPs were stable over 4 days after preparation and ~3 days after subjecting to all relevant biological fluids. The AuNPs capped with WCS-GA-DBBN peptide exhibited superior cellular internalization into prostate tumor (PC-3) cells with evidence of receptor mediated endocytosis. Conclusion:The AuNPs capped with WCS-GA-DBBN exhibited selective affinity toward prostate cancer cells. AuNPs conjugated with WCS-GA-DBBN serve as a new generation of theranostic agents for treating various neoplastic diseases, thus opening-up new applications in oncology.

Chitosan‐grafted‐polyethylene (CS‐g‐PE) film was prepared using simultaneous radiation‐inducing grafting technique. The copper ion (Cu2+) adsorptivity on the CS‐g‐PE film was determined. The CS‐hydroxybenzyltriazole (CS‐HOBt), CS‐N‐hydroxysuccinimide (CS‐NHS), CS‐acetic acid (CS‐HOAc), and CS‐glutathione (CS‐GSH) were used as CS‐salts in aqueous solutions. Among these grafting solution systems, the CS‐g‐PE film prepared from CS‐HOBt solution showed the greatest grafting amount and highest Cu2+ adsorptivity, up to 30.2% (1.51 ppm, 7.56 µg cm−2). The effects of the CS‐HOBt concentration and mixing solution on the grafting amount were also observed to clarify their efficacies to assist radiation‐induced grafting reaction. SEM/EDS mapping, ICP and XRF were used to clarify the Cu2+ adsorption capacity of the CS‐g‐PE film and the stability of Cu2+ on the CS‐g‐PE complex film. The Cu2+ showed its stability on the CS‐g‐PE film at room temperature in neutral and basic solutions. The Cu2+‐‐‐CS‐g‐PE complex film reduced pest snail breeding as high as 54%. The success of this observation is a new approach to modify PE surface with a functional biopolymer, CS containing Cu2+ complex for controlling pest snail breeding. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 41204.

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