Terezinha de Jesus Andreoli Pinto

Dr. Terezinha de Jesus Andreoli Pinto

Department of Pharmacy, Faculty of Pharmaceutical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, 05508-000 São Paulo, Brazil

Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 July 2015 in International Journal of Cosmetic Science
Verified
Journal Article
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MYM. N. Yukuyama
M. N. Yukuyama
DGD. D. M. Ghisleni
D. D. M. Ghisleni
Terezinha de Jesus Andreoli PintoTerezinha de Jesus Andreoli Pinto
Terezinha de Jesus Andreoli Pinto
NBN. A. Bou‐Chacra
N. A. Bou‐Chacra

16 December 2017 in Journal of Biomedical Materials Research Part B: Applied Biomaterials
Verified
Journal Article
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RGRaquel Galante
Raquel Galante
Terezinha de Jesus Andreoli PintoTerezinha de Jesus Andreoli Pinto
Terezinha de Jesus Andreoli Pinto
Rogerio ColacoRogerio Colaco
Rogerio Colaco
Ana Paula SerroAna Paula Serro
Ana Paula Serro

1 March 2006 in Brazilian Journal of Microbiology
Verified
Journal Article
Open access
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ABAdriana Bugno
Adriana Bugno
AAAdriana Aparecida Buzzo Almodovar
Adriana Aparecida Buzzo Almodovar
TPTatiana Caldas Pereira
Tatiana Caldas Pereira
Terezinha de Jesus Andreoli PintoTerezinha de Jesus Andreoli Pinto
Terezinha de Jesus Andreoli Pinto
MSMyrna Sabino
Myrna Sabino
The increase in the consumption of natural drugs have made their use a Public Health problem due to the possibility of access to products without adequate conditions of use. The concern with the quality of the natural products is due to the potential fungal contamination and the risk of the presence of mycotoxins. Ninety-one samples of medicinal plants were evaluated for the fungal contamination and the mycotoxigenic potential of Aspergillus and Penicillium isolated from the samples. Results indicated that predominant mycoflora was distributed in 10 genera. From these, 89.9% of the isolates corresponded to genera Aspergillus and Penicillium, which are extremely important from the mycotoxicological standpoint. 21.97% of the Aspergillus and Penicillium isolates proved to have the ability for producing aflatoxins (42.9%), ochratoxin A (22.4%) and citrinine (34.7%). The presence of toxigenic moulds represents a potential risk of mycotoxin contamination and considering the worldwide increased use of herbal products as alternative medicines, it is necessary setting standards for toxigenic moulds in crude herbal drugs in order to reduce the risks for consumers' health. O aumento no consumo de produtos naturais transformou seu uso em um problema de Saúde Pública devido a possibilidade do acesso a produtos sem adequadas condições de uso. A preocupação com a qualidade dos produtos naturais é devida à potencialidade de contaminação por fungos e ao risco da presença de micotoxinas. Noventa e uma amostras de plantas medicinais foram avaliadas quanto à contaminação fungica e ao potencial micotoxigênico de Aspergillus e Penicillium isolados nestas amostras. Os resultados indicaram que a micoflora predominante esteve distribuída entre 10 gêneros. Entretanto, 89,9% dos isolados corresponderam aos gêneros Aspergillus e Penicillium, extremamente importantes do ponto de vista micotoxicológico. Verificou-se que 21,97% dos isolados de Aspergillus e Penicillium demonstraram capacidade para produzir aflatoxinas (42,9%), ocratoxina A (22,4%) e citrinina (34,7%). A presença de fungos toxigênicos representa risco potencial de contaminação com micotoxinas e considerando o aumento no consumo de produtos de origem vegetal como alternativa terapêutica, é necessário estabelecer padrões para a presença de fungos toxigênicos em drogas vegetais a fim de reduzir os riscos à saúde do consumidor

1 November 2018 in Biomedicine & Pharmacotherapy
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Journal Article
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Kamal DuaKamal Dua
Kamal Dua
VRVamshi Krishna Rapalli
Vamshi Krishna Rapalli
SSShakti Shukla
Shakti Shukla
GSGautam Singhvi
Gautam Singhvi
MSMadhur D. Shastri
Madhur D. Shastri
PHPhilip M. Hansbro
Philip M. Hansbro

1 September 2016 in European Polymer Journal
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Journal Article
Closed access
CRCarolina Fracalossi Rediguieri
Carolina Fracalossi Rediguieri
RSRogério Corte Sassonia
Rogério Corte Sassonia
Kamal DuaKamal Dua
Kamal Dua
IKIrene Satiko Kikuchi
Irene Satiko Kikuchi
Terezinha de Jesus Andreoli PintoTerezinha de Jesus Andreoli Pinto
Terezinha de Jesus Andreoli Pinto

1 January 2013 in BioMed Research International
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Journal Article
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YGYuan Gao
Yuan Gao
JZJieyu Zuo
Jieyu Zuo
NBNadia Bou-Chacra
Nadia Bou-Chacra
Terezinha de Jesus Andreoli PintoTerezinha de Jesus Andreoli Pinto
Terezinha de Jesus Andreoli Pinto
SCSophie-Dorothee Clas
Sophie-Dorothee Clas
Raimar LöbenbergRaimar Löbenberg
Raimar Löbenberg
The aim of this study was to assess thein vitrorelease kinetics of antituberculosis drug-loaded nanoparticles (NPs) using a “modified” cylindrical apparatus fitted with a regenerated cellulose membrane attached to a standard dissolution apparatus (modifiedcylinder method). The model drugs that were used were rifampicin (RIF) and moxifloxacin hydrochloride (MX). Gelatin and polybutyl cyanoacrylate (PBCA) NPs were evaluated as the nanocarriers, respectively. The dissolution and release kinetics of the drugs from loaded NPs were studied in different media using the modified cylinder method and dialysis bag technique was used as the control technique. The results showed that use of the modified cylinder method resulted in different release profiles associated with unique release mechanisms for the nanocarrier systems investigated. The modified cylinder method also permitted discrimination between forced and normalin vitrorelease of the model drugs from gelatin NPs in the presence or absence of enzymatic degradation. The use of dialysis bag technique resulted in an inability to differentiate between the mechanisms of drug release from the NPs in these cases. This approach offers an effective tool to investigatein vitrorelease of RIF and MX from NPs, which further indicate that this technique can be used for performance testing of nanosized carrier systems.