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DOI 10.1016/j.bmcl.2016.02.047

Медицинская библиотека · Bioorganic & medicinal chemistry letters · 2016

Carbon nanodots as molecular scaffolds for development of antimicrobial agents.

Ngu-Schwemlein Maria, Chin Suk Fun, Hileman Ryan, Drozdowski Chris, Upchurch Clint, Hargrove April

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

We report the potential of carbon nanodots (CNDs) as a molecular scaffold for enhancing the antimicrobial activities of small dendritic poly(amidoamines) (PAMAM). Carbon nanodots prepared from sago starch are readily functionalized with PAMAM by using N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS). Electron microscopy images of these polyaminated CNDs show that they are approximately 30-60nm in diameter. Infrared and fluorescence spectroscopy analyses of the water-soluble material established the presence of the polyamidoaminated moiety and the intrinsic fluorescence of the nanodots. The polyaminated nanodots (CND-PAM1 and CND-PAM2) exhibit in vitro antimicrobial properties, not only to non-multidrug resistant bacteria but also to the corresponding Gram-negative multidrug bacteria. Their minimum inhibitory concentration (MIC) ranges from 8 to 64μg/mL, which is much lower than that of PAMAM G1 or the non-active PAMAM G0 and CNDs. Additionally, they show synergistic effect in combination with tetracycline or colistin. These preliminary results imply that CNDs can serve as a promising scaffold for facilitating the rational design of antimicrobial materials for combating the ever-increasing threat of antibiotic resistance. Moreover, their fluorescence could be pertinent to unraveling their mode of action for imaging or diagnostic applications.

Для цитирования: Ngu-Schwemlein Maria, Chin Suk Fun, Hileman Ryan, Drozdowski Chris, Upchurch Clint, Hargrove April. Carbon nanodots as molecular scaffolds for development of antimicrobial agents.. Bioorganic & medicinal chemistry letters. 2016. DOI: 10.1016/j.bmcl.2016.02.047.

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