Novel phthalocyanines activated by dim light for mosquito larva- And cell-inactivation with inference for their potential as broadspectrum photodynamic insecticides
Journal
PLoS ONE
Journal Volume
14
Journal Volume
14
Journal Issue
5
Journal Issue
5
Pages
e0217355
Start Page
e0217355
Date Issued
2019
Author(s)
Abstract
Mosquitoes are significant vectors, responsible for transmitting serious infectious diseases, including the recent epidemics of global significance caused by, for example, Zika, Dengue and Chikungunya viruses. The chemical insecticides in use for mosquito control are toxic and ineffective due to the development of resistance to them. The new approach to reduce mosquito population by releasing genetically modified males to cause female infertility is still under environmental safety evaluation. Photodynamic insecticides (PDI) have long been known as a safe and effective alternative by using dyes as the photosensitizers (PS) for activation with light to generate insecticidal singlet oxygen and reactive oxygen species. This approach warrants re-examination with advances in the chemical synthesis of novel PS, e.g. phthalocyanines (PC). Nine PC were compared with five porphyrin derivatives and two classic PS of halogenated fluoresceins, i.e. cyanosine and rose bengal experimentally for photodynamic treatment (PDT) of the larvae of laboratory-reared Aedes mosquitoes and their cell lines. Groups of 2nd instar larvae were first exposed overnight to graded concentrations of each PS in the dark followed by their exposure to dim light for up to 7 hours. Larvae of both experimental and control groups were examined hourly for viability based on their motility. Monolayers of mosquito cells were similarly PS-sensitized and exposed briefly to light at the PS-specific excitation wavelengths. Cell viability was assessed by MTT reduction assays. Of the 16 PS examined for photodynamic inactivation of the mosquito larvae, effective are three novel PC, i.e. amino-Si-PC1 and -PC2, anilinium Zn-PC3.4, pyridyloxy SiPC14 and two porphyrin derivatives, i.e. TPPS2 and TMAP. Their EC50 values were determined, all falling in the nanomolar range lower than those of rose bengal and cyanosine. All PS effective in vivo were also found to dose-dependently inactivate mosquito cells photodynamically in vitro, providing cellular basis for their larvicidal activities. The present findings of novel PC with effective photodynamic larvicidal activities provide fresh impetus to the development of PDI with their established advantages in safety and efficacy. Toward that end, the insect cell lines are of value for rapid screening of new PC. The optimal excitability of PC with insect-invisible red light is inferred to have the potential to broaden the range of targetable insect pests. ? 2019 Shiao et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
SDGs
Other Subjects
cyanosine; fluorescein derivative; insecticide; photodynamic insecticide; phthalocyanine derivative; porphyrin derivative; protoporphyrin; rose bengal; unclassified drug; indole derivative; insecticide; photosensitizing agent; phthalocyanine; porphyrin; Aedes aegypti; Aedes albopictus; animal cell; animal experiment; Article; cell motility; cell viability; concentration (parameter); concentration response; controlled study; dose response; EC50; female; in vitro study; in vivo study; larva; larvicidal activity; light; light exposure; male; mouse; MTT assay; nonhuman; photodynamic therapy; photodynamics; Aedes; animal; drug effect; metabolism; mosquito control; mosquito vector; procedures; Aedes; Animals; Indoles; Insecticides; Larva; Mosquito Control; Mosquito Vectors; Photosensitizing Agents; Porphyrins
Publisher
Public Library of Science
Type
journal article