scholarly journals Curcumin-removed turmeric oleoresin nano-emulsion as a novel botanical fungicide to control anthracnose (Colletotrichum gloeosporioides) in litchi

2021 ◽  
Vol 10 (1) ◽  
pp. 729-741
Author(s):  
Van Cuong Bui ◽  
The Tam Le ◽  
Tuyen Hong Nguyen ◽  
Nam Thi Pham ◽  
Hoang Dinh Vu ◽  
...  
Keyword(s):  
Field Trial ◽  
Colletotrichum Gloeosporioides ◽  
Inhibitory Concentration ◽  
Particle Sizes ◽  
Control Efficacy ◽  
Potent Inhibition ◽  
Nano Emulsion ◽  
Nano Formulation

Abstract During curcumin production in Vietnam, curcumin-removed turmeric oleoresin (CRTO) has been considered as a by-product. It costs to treat the by-product to prevent environmental pollution. In this study, the by-product was utilized as an active ingredient for preparing a botanical fungicide-based nano-emulsion and evaluated for its in vitro and in vivo control efficacy against Colletotrichum gloeosporioides, a causal agent of anthracnose of litchi, in the laboratory as well as a field trial. The nano-emulsion is colloidally stable and uniform with particle sizes of 95–250 nm. CRTO nano-emulsion significantly affected various Colletotrichum species. Notably, this nano-emulsion showed potent inhibition for the mycelial growth of C. gloeosporioides and solidly suppressed the development of anthracnose on litchi fruits. In the in vitro inhibition test, the equivalent half-maximal inhibitory concentration of CRTO in nano-formulation was 0.11 mg·mL−1, which was 3.0× and 6.1× lower than IC50 values of CRTO alone (0.33 mg·mL−1) and a mixture of curcuminoids (0.48 mg·mL−1), respectively. In the field trial, the litchi anthracnose infection was effectively controlled by nano-formulation. These results suggest that CRTO nano-emulsion could be used as an alternative to harmful synthetic fungicides to control anthracnose on litchi fruits.

scholarly journals Characterization of LDD-2633 as a Novel RET Kinase Inhibitor with Anti-Tumor Effects in Thyroid Cancer

2021 ◽  
Vol 14 (1) ◽  
pp. 38
Author(s):  
Hyo Jeong Lee ◽  
Pyeonghwa Jeong ◽  
Yeongyu Moon ◽  
Jungil Choi ◽  
Jeong Doo Heo ◽  
...  
Keyword(s):  
Thyroid Cancer ◽  
Thyroid Carcinoma ◽  
Kinase Inhibitor ◽  
Point Mutations ◽  
Carcinoma Cells ◽  
Medullary Thyroid ◽  
Potent Inhibition ◽  
Kinase Inhibitory Activity

Rearranged during transfection (RET), a receptor tyrosine kinase, is activated by glial cell line-derived neurotrophic factor family ligands. Chromosomal rearrangement or point mutations in RET are observed in patients with papillary thyroid and medullary thyroid carcinomas. Oncogenic alteration of RET results in constitutive activation of RET activity. Therefore, inhibiting RET activity has become a target in thyroid cancer therapy. Here, the anti-tumor activity of a novel RET inhibitor was characterized in medullary thyroid carcinoma cells. The indirubin derivative LDD-2633 was tested for RET kinase inhibitory activity. In vitro, LDD-2633 showed potent inhibition of RET kinase activity, with an IC50 of 4.42 nM. The growth of TT thyroid carcinoma cells harboring an RET mutation was suppressed by LDD-2633 treatment via the proliferation suppression and the induction of apoptosis. The effects of LDD-2633 on the RET signaling pathway were examined; LDD-2633 inhibited the phosphorylation of the RET protein and the downstream molecules Shc and ERK1/2. Oral administration of 20 or 40 mg/kg of LDD-2633 induced dose-dependent suppression of TT cell xenograft tumor growth. The in vivo and in vitro experimental results supported the potential use of LDD-2633 as an anticancer drug for thyroid cancers.

The in vitro efficacy of neutral electrolysed water and povidone-iodine against CRS-associated biofilms

2021 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
C.A. Lux ◽  
K. Biswas ◽  
M.W. Taylor ◽  
R.G. Douglas
Keyword(s):  
Inhibitory Concentration ◽  
Povidone Iodine ◽  
Minimum Bactericidal Concentration ◽  
Treatment Options ◽  
Antimicrobial Treatment ◽  
Biofilm Reactor ◽  
Bacterial Biofilms ◽  
Antibiofilm Activity

Background: Despite best medical and surgical practice, some cases of chronic rhinosinusitis (CRS) can remain recalcitrant. Bacterial biofilms have been associated with the recalcitrance of sinonasal inflammation. Biofilms are highly resistant to commonly prescribed antibiotics. Accordingly, more effective antimicrobial treatment options are needed to treat refractory CRS. The aim of this study was to determine the in vitro efficacy of neutral electrolysed water (NEW) and povidone-iodine (PVI) against CRS-associated Staphylococcus aureus biofilms. Methods: Mature S. aureus biofilms were grown in a Centre for Disease Control (CDC) biofilm reactor. The antimicrobial activity of NEW, PVI and doxycycline was determined for both planktonic and biofilm cultures of a clinical S. aureus isolate using minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and minimum biofilm eradication concentration (MBEC) assays. Results: MICs and MBCs were determined for all antimicrobials. MBC values were similar to MICs for both antiseptics, but doxycycline MBCs were significantly higher than the associated MICs. Biofilms were highly resistant to NEW and doxycycline. The MBEC for doxycycline was between 500 and 1000 µg/mL. NEW was ineffective against biofilms and no MBEC could be determined. In contrast, a concentration of 10% of the commercial PVI solution (10 mg/mL PVI) led to effective eradication of mature biofilms. Conclusion: In this study, only PVI showed promising antibiofilm activity at physiological concentrations. The in vivo efficacy of PVI warrants further investigation of its potential as a treatment for recalcitrant CRS.

scholarly journals Bioatividade de indutores de resistência no manejo da antracnose da goiabeira (Psidium guajava L.)

2016 ◽  
Vol 42 (2) ◽  
pp. 149-154 ◽  
Author(s):  
Rommel dos Santos Siqueira Gomes ◽  
Andréa Celina Ferreira Demartelaere ◽  
Luciana Cordeiro do Nascimento ◽  
Wendel Oliveira Maciel ◽  
Danilo Bruno Néri da Silva Wanderley
Keyword(s):  
Colletotrichum Gloeosporioides ◽  
Psidium Guajava

RESUMO A cultura da goiaba apresenta perdas em torno de 40 a 60% na pós-colheita relacionadas a problemas fitossanitários, como a antracnose causada pelo fungo Colletotrichum gloeosporioides. Pesquisas com métodos alternativos utilizando indutores de resistência têm sido bastante promissoras na busca de produtos com alto potencial no controle de patógenos em pós-colheita. Assim, o presente trabalho teve como objetivo avaliar os indutores de resistência no controle da antracnose e seus efeitos na qualidade físico-química em frutos de goiabeira ‘Paluma’. Os tratamentos utilizados foram: Agro-mós®, Ecolife®, Fosfitonova K®, Cuprogarb 500®, Rocksil® e testemunha (água destilada esterilizada). Realizou-se o teste in vitro, com discos de colônia de C. gloeosporioides (0,45 cm de diâmetro) com sete dias de cultivo e, postos em meio de cultura BDA acrescidos com os indutores. Foi determinada a porcentagem de inibição do crescimento micelial de C. gloeosporioides. O ensaio in vivo foi realizado com frutos de goiabeira variedade Paluma, desinfestados e tratados com indutores. Em seguida, discos de colônia do C. gloeosporioides foram inoculados e do primeiro ao oitavo dia após a inoculação, foram feitas avaliações do diâmetro das lesões nos frutos. As análises pós-colheita foram realizadas, avaliando a perda de massa fresca, sólidos solúveis totais (SST), acidez titulável (AT), razão SST/AT e potencial hidrogeniônico (pH). Foi utilizado o delineamento inteiramente casualizado, em esquema de parcela subdivididas 6x8 (tratamentos x período de avaliação) e as médias comparadas pelo teste de Tukey a 5% de probabilidade. Os indutores Agro-mos®, Ecolife®, Fosfitonova K®, Cuprogarb 500® e Rocksil® inibiram o crescimento micelial do C. gloeosporioides in vitro, reduziram o diâmetro das lesões e mantiveram a qualidade pós-colheita em frutos de goiabeira ‘Paluma’.

scholarly journals Efeito fungitóxico do óleo essencial de aroeira da praia (Schinus terebinthifolius RADDI) sobre Colletotrichum gloeosporioides

2013 ◽  
Vol 15 (1) ◽  
pp. 150-157 ◽  
Author(s):  
L.F.G Oliveira Junior ◽  
R.B. Santos ◽  
F.O. Reis ◽  
S.T Matsumoto ◽  
W.M.S. Bispo ◽  
...  
Keyword(s):  
Colletotrichum Gloeosporioides ◽  
Tween 80 ◽  
Schinus Terebinthifolius

Neste trabalho foi avaliado o efeito do óleo essencial do fruto de Schinus terebinthifolius sobre o crescimento micelial do fungo Colletotrichum gloeosporioides in vitro, e no desenvolvimento da antracnose no período de pós-colheita em mamões. As diferentes concentrações de óleo foram diluídas em Tween 80 a 8%. No experimento in vitro foram preparados meios de cultura BDA nas concentrações de 0,05; 0,10; 0,25 e 0,50% do óleo essencial. O controle negativo foi realizado apenas com meio BDA e o controle solvente com meio BDA e Tween 80 a 8%. A inibição do crescimento do fungo foi diretamente proporcional à quantidade do óleo e a maior inibição encontrada foi de 79,07% na concentração de óleo de 0,50%. No experimento in vivo os frutos do mamoeiro foram inoculados com o fungo em quatro tratamentos: com biofilme; com biofilme mais 0,50% do óleo; com fungicida Prochloraz e frutos controle. Embora o tratamento com óleo tenha sido eficiente contra o fungo, não foi indicado comercialmente, pois apresentou valores elevados de perda de massa fresca, de firmeza, e também sintomas de fitotoxidade. O óleo tem propriedade antifúngica contra C. gloeosporioides in vitro e in vivo, contudo, não é recomendado para o mamão em função da fitotoxidez

scholarly journals Efeito In vitro e In vivo de filtrados de rizobactérias sobre Colletotrichum gloeosporioides Penz. do cafeeiro

2005 ◽  
Vol 29 (3) ◽  
pp. 553-561
Author(s):  
Gilvane Aparecida de Carvalho ◽  
Mário Sobral de Abreu ◽  
Denilson Ferreira de Oliveira ◽  
Mário Lúcio Vilela de Resende ◽  
Maria Floriana Esteves de Abreu
Keyword(s):  
Colletotrichum Gloeosporioides

Objetivou-se avaliar o efeito de filtrados derivados de culturas de rizobactérias na inibição da germinação de esporos de Colletotrichum gloeosporioides e confirmar sua ação antifúngica em relação à mancha manteigosa em mudas de cafeeiro. Foram conduzidos ensaios in vitro para testar 42 filtrados, identificando-se os de maior capacidade de inibir a germinação de esporos do fungo. Plântulas de café foram submetidas à inoculação com Colletotrichum e pulverização com quatro dos filtrados mais promissores. Os tratamentos constituíram um fatorial 4x4+2, combinando a aplicação de quatro filtrados com quatro modos de inoculação do fungo (ausência de inoculação e inoculação dois dias antes, junto, ou dois dias depois da aplicação dos filtrados). Uma testemunha absoluta e outra que recebeu somente o inóculo do fungo constituíram tratamentos adicionais. Após 35 dias, foram avaliados o crescimento do cafeeiro e a severidade da mancha manteigosa. Os filtrados apresentaram ampla variação quanto à atividade antifúngica in vitro e cinco deles inibiram completamente a germinação dos esporos. No experimento com planta, os filtrados tiveram eficácia similar contra a mancha manteigosa, com controle parcial da doença (35%). A aplicação dos filtrados teve efeito depressivo ao crescimento do cafeeiro, proporcionando menor produção de matéria seca em relação à testemunha absoluta.

scholarly journals Antiparasitary Activity Of The Juglone Compound: A Narrative Review

2021 ◽  
pp. 13
Author(s):  
◽  
Keyword(s):  
Mortality Rate ◽  
Leishmania Donovani ◽  
Inhibitory Concentration ◽  
Narrative Review ◽  
Hymenolepis Nana ◽  
Compound A ◽  
Living Organisms ◽  
Nanomolar Range

Objective: To report, based on the literature, the action of the compound 5-hydroxy-1,4-naphthoquinone against parasites (protozoa and helminths) that affect humans. Methods: This is a narrative review that used Pubmed and Google Scholar as a data tool. This work included articles published until September 2020 that were directly related to the use of the compound juglone in antiparasitic trials. Results: The compound juglone demonstrated promising effects as a human and animal antiparasitic substance. In protozoa, the Apicomplexo Toxoplasma gondii parasite showed a high mortality rate in concentrations of juglone in the nanomolar range. The juglone showed an average inhibitory concentration (IC50) of 1.62 µM, >100 µM, and 2.02 µM µM for Trypanosoma cruzi, T. brucei rhodesiense, and Leishmania donovani, respectively. Also, the juglone showed antihelmintic activity on Hymenolepis nana in mice, and on adult worms of Schistosoma mansoni (LE strain) with IC50 34.16 µM, 32.14 µM, and 25 µM in the 24h, 48h, and 72 h, respectively. Conclusion: The results published so far show the in vitro antiparasitic potential of juglone, and the need for further studies on the specific mode of action that interacts with parasites. Besides, the literature is still limited to studies that evaluate in vivo the compound juglone, requiring better information on its interaction with living organisms.

scholarly journals Synergistic Effects of Curcumin and Nano-Curcumin against Toxicity, Carcinogenicity, and Oxidative Stress Induced by Tartrazine at Normal and Cancer Cell Levels

Catalysts ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1203
Author(s):  
Gaber E. El-Desoky ◽  
Saikh M. Wabaidur ◽  
Mohamed A. Habila ◽  
Zeid A. AlOthman
Keyword(s):  
Oxidative Stress ◽  
Synergistic Effects ◽  
Economic Benefits ◽  
Cellular Level ◽  
Anticancer Properties ◽  
Antioxidant Defense Enzymes ◽  
Apoptosis Protein ◽  
Nano Formulation

In this study, the cellular synergistic and antagonistic effects of mixing tartrazine (TZ) with curcumin (CUR) or curcumin-nanoparticles (CUR-NPs) were investigated. The in vivo administration of TZ, CUR, CUR-NPs, and TZ mixed with CUR or CUR-NPs at 75:25 or 50:50 ratios were tested. The results indicated that CUR and CUR -NPs reduced the cytotoxicity effects of TZ on skin fibroblast BJ-1 (ATCC® CRL-2522™) normal cells. However, among the tested materials, CUR-NPs had highest in vitro and in vivo antioxidant activity compared to TZ. Furthermore, CUR-NPs and CUR exhibited anticancer activity against HepG-2 liver cancer cells via apoptosis induction. The key apoptosis protein genes Caspase-3, p53, and Bax were upregulated, whereas Bc-2, which exhibits anti-apoptosis activity, was downregulated. Our results indicated that the nano-formulation of CUR alters its physicochemical properties, including the size and shape, and increases its antioxidant and anticancer properties. CUR-NPs also overcome the side effect of using TZ as a yellow color and food preservative additive, due to its reduced toxicity, oxidative stress, and carcinogenicity. In agreement with our previous findings, CUR and CUR-NPs were able to protect against cellular oxidative stress by stimulating endogenous antioxidant defense enzymes, including superoxide dismutase (SOD), catalase (CAT), reduced glutathione (GSH), glutathione peroxidase (GPx), and glutathione-S-transferase (GST). We conclude that the nano-formulation of CUR exhibits economic benefits as a new strategy to use CUR as a food additive at the cellular level.

scholarly journals Mesyl phosphoramidate backbone modified antisense oligonucleotides targeting miR-21 with enhanced in vivo therapeutic potency

2020 ◽  
Vol 117 (51) ◽  
pp. 32370-32379
Author(s):  
Olga A. Patutina ◽  
Svetlana K. Gaponova (Miroshnichenko) ◽  
Aleksandra V. Sen’kova ◽  
Innokenty A. Savin ◽  
Daniil V. Gladkikh ◽  
...  
Keyword(s):  
Tumor Model ◽  
Rnase H ◽  
Mouse Tumor ◽  
Internal Organs ◽  
Potent Inhibition ◽  
Nuclease Resistance ◽  
New Type

The design of modified oligonucleotides that combine in one molecule several therapeutically beneficial properties still poses a major challenge. Recently a new type of modified mesyl phosphoramidate (or µ-) oligonucleotide was described that demonstrates high affinity to RNA, exceptional nuclease resistance, efficient recruitment of RNase H, and potent inhibition of key carcinogenesis processes in vitro. Herein, using a xenograft mouse tumor model, it was demonstrated that microRNA miR-21–targeted µ-oligonucleotides administered in complex with folate-containing liposomes dramatically inhibit primary tumor growth via long-term down-regulation of miR-21 in tumors and increase in biosynthesis of miR-21–regulated tumor suppressor proteins. This antitumoral effect is superior to the effect of the corresponding phosphorothioate. Peritumoral administration of µ-oligonucleotide results in its rapid distribution and efficient accumulation in the tumor. Blood biochemistry and morphometric studies of internal organs revealed no pronounced toxicity of µ-oligonucleotides. This new oligonucleotide class provides a powerful tool for antisense technology.

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