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J. Campos

Researcher at University of Porto

Publications -  15
Citations -  214

J. Campos is an academic researcher from University of Porto. The author has contributed to research in topics: Chemistry & TBARS. The author has an hindex of 6, co-authored 14 publications receiving 138 citations. Previous affiliations of J. Campos include Fernando Pessoa University.

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Acute effects of tetracycline exposure in the freshwater fish Gambusia holbrooki: antioxidant effects, neurotoxicity and histological alterations.

TL;DR: The obtained results suggest the existence of a cause-and-effect relationship between the exposure to tetracycline and histological alterations and enzymatic activity indicating that this compound can exert a pro-oxidative activity.
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Ecotoxicological effects of salicylic acid in the freshwater fish Salmo trutta fario: antioxidant mechanisms and histological alterations

TL;DR: Brown trout individuals were chronically exposed to Salicylic acid in order to evaluate the enzymatic and histological effects, in both gills and liver, and showed the occurrence of oxidative stress, reflected by an increased activity of GPx and GRed in the liver.
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Ecotoxicological effect of zinc pyrithione in the freshwater fish Gambusia holbrooki

TL;DR: The present work assesses the potential ecotoxicity elicited by zinc pyrithione in the freshwater fish Gambusia holbrooki after an acute (96 h) exposure and examines biomarkers indicating the occurrence of pro-oxidative effects, suggesting that the oxidative pathway is not the major toxicological outcome of exposure to zinc pithione.
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Discovery of a New Xanthone against Glioma: Synthesis and Development of (Pro)liposome Formulations.

TL;DR: The new xanthone 2 was still able to inhibit the growth of glioblastoma cells after liposome formulation, and showed significantly higher stability, at the expense of losing its biocompatibility as a drug carrier in higher concentrations.
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Swellable polymeric particles for the local delivery of budesonide in oral mucositis.

TL;DR: This work proposes the development of a biocompatible delivery system with boosted abilities of retention and control release of budesonide, a corticosteroid with an elevated ratio of topical anti-inflammatory to systemic action.