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Dive into the research topics where Maria Rose Jane R. Albuquerque is active.

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Featured researches published by Maria Rose Jane R. Albuquerque.


Molecules | 2010

Casbane diterpene as a promising natural antimicrobial agent against biofilm-associated infections

Victor Alves Carneiro; Hélcio Silva dos Santos; Francisco Vassiliepe Sousa Arruda; Paulo Nogueira Bandeira; Maria Rose Jane R. Albuquerque; Maria Olívia Pereira; Mariana Henriques; Benildo Sousa Cavada; Edson Holanda Teixeira

Croton nepetaefolius is a native plant from northeastern Brazil that belongs to the Euphorbiaceae family. The biological action of this plant has been extensively explored, being the secondary metabolites responsible for its properties alkaloids, diterpenes, and triterpenes. This study aimed to evaluate the ability of casbane diterpene (CD), isolated from the ethanolic extract of C. nepetaefolius, to inhibit microbial growth and biofilm formation of several clinical relevant species (bacteria and yeasts). It was found that CD possessed biocidal and biostatic activity against the majority of the species screened, with minimal active concentrations ranging between 125 and 500 µg/mL. In addition, it was observed that biofilm formation was inhibited even when the planktonic growth was not significantly affected. In conclusion, CD showed potential to be a natural tool for the treatment of diseases caused by different infectious microorganisms.


Archives of Oral Biology | 2012

Antimicrobial and antibiofilm action of Casbane Diterpene from Croton nepetaefolius against oral bacteria.

Nairley Cardoso Sá; Theodora Thays Arruda Cavalcante; Amanda Ximenes Araújo; Hélcio Silva dos Santos; Maria Rose Jane R. Albuquerque; Paulo Nogueira Bandeira; Rodrigo Maranguape Silva da Cunha; Benildo Sousa Cavada; Edson Holanda Teixeira

OBJECTIVE The antibacterial activity of Casbane Diterpene (CD) was evaluated in vitro against Streptococcus oralis, S. mutans, S. salivarius, S. sobrinus, S. mitis and S. sanguinis. The viability of planktonic cells was analysed by susceptibility tests (MIC and MBC) and antibiofilm action was assayed. METHODS The minimal inhibitory and bactericidal concentrations (MIC and MBC) of oral Streptococcus were evaluated through microdilution tests. To assay antibiofilm activity, biofilms were generated on 96-wells polystyrene plates under the presence of CD and quantified by a crystal violet technique and colonies forming units counting. RESULTS The CD isolated from Croton nepetaefolius showed antimicrobial effect on planktonic forms and biofilms of oral pathogens, with MIC values of 62.5 μg/mL against Streptococcus oralis and values between 125 and 500 μg/mL against S. mutans, S. salivarius, S. sobrinus, S. mitis and S. sanguinis. CD showed an inhibitory effect on S. mutans biofilm formation at 250 μg/mL, and a decrease on viable cell of 94.28% compared to the normal biofilm growth. CONCLUSIONS The compound CD can be considered as a promising molecule for the treatment against oral pathogens responsible for dental biofilm.


Bioorganic & Medicinal Chemistry | 2011

Amyrin esters induce cell death by apoptosis in HL-60 leukemia cells

Francisco W.A. Barros; Paulo Nogueira Bandeira; Daisy Jereissati Barbosa Lima; Assuero Silva Meira; Silvana S. de Farias; Maria Rose Jane R. Albuquerque; Hélcio Silva dos Santos; Telma L. G. Lemos; Manoel Odorico de Morais; Letícia V. Costa-Lotufo; Cláudia Pessoa

Four derivatives of an α,β-amyrin mixture were synthesized by acylation with appropriate anhydrides. The structures of the compounds were confirmed by means of IR and (1)H and (13)C NMR. The compounds were screened for cytotoxic activity using four human tumor cell lines (HL-60, MDAMB-435, SF-295 and HCT-8) and normal peripheral blood mononuclear cells (PBMC). 3-O-Carboxymaleinate of α,β-amyrin (3a/3b) were found to be the only active compounds of the series (high cytotoxicity), showing IC(50) values ranging from 1.8 to 3μM. In PBMC, 3a/3b were not toxic, suggesting selectivity for tumor cells. To better understand the mechanism of action involved in the cytotoxicity of 3a/3b, HL-60 cells treated with 3a/3b were examined for morphological changes, DNA fragmentation, cell cycle perturbation, externalization of phosphatidylserine and activation of caspases 3/7, with doxorubicin serving as the positive control. The results indicate that the cytotoxicity of 3a/3b involves the induction of cell death by apoptosis.


Anais Da Academia Brasileira De Ciencias | 2007

Nematicidal and larvicidal activities of the essential oils from aerial parts of Pectis oligocephala and Pectis apodocephala Baker

Maria Rose Jane R. Albuquerque; Sônia Maria O. Costa; Paulo Nogueira Bandeira; Gilvandete Maria Pinheiro Santiago; Manoel Andrade-Neto; Edilberto R. Silveira; Otília Deusdênia L. Pessoa

The chemical composition of the essential oils from aerial parts of Pectis apodocephala and Pectis oligocephala were analyzed by GC-MS. The essential oils of these species were predominantly constituted by monoterpenes. Geranial (42.9-44.5%), neral (32.2-34.2%) and alpha-pinene (10.7-11.4%) were the main constituents in the oil of P. apodocephala, while p-cymene (50.3-70.9%) and thymol (24.4-44.7%), were the prevalent compounds in the oil of P. oligocephala. The essential oils were tested against the root knot nematode Meloidogyne incognita and Aedes aegypti larvae survival. The results obtained show that both essential oils exhibited significant activity and could be considered as potent natural namaticidal and larvicidal agents.


Journal of Natural Products | 2009

Cytotoxic Diterpenoids from Croton argyrophylloides

Hélcio Silva dos Santos; Francisco W.A. Barros; Maria Rose Jane R. Albuquerque; Paulo Nogueira Bandeira; Cláudia Pessoa; Raimundo Braz-Filho; Francisco José Queiroz Monte; José Henrique Leal-Cardoso; Telma L. G. Lemos

Two new diterpenes, 1 and 2, together with the known ent-15-oxo-kaur-16-en-18-oic acid (3), were isolated from the bark of Croton argyrophylloides. The structural characterization of 1 and 2 was determined on the basis of spectroscopic data interpretation. The cytotoxicity of each compound was evaluated against HL-60 (leukemia), MDAMB-435 (melanoma), SF-295 (glioblastoma), and HCT-8 (colon carcinoma) human tumor cell lines and against human peripheral blood mononuclear cells. The hemolytic potential in mouse erythrocytes was also tested for 1-3.


Química Nova | 2010

Óleos essenciais das folhas de Vernonia Remotiflora e Vernonia Brasiliana: composição química e atividade biológica

Ana Isabel V. Maia; Maria Conceição M. Torres; Otília Deusdênia L. Pessoa; Jane Eire Silva Alencar de Menezes; Sônia Maria O. Costa; Vanessa Lúcia Rodrigues Nogueira; Vânia Maria Maciel Melo; Elnatan Bezerra de Souza; Maria Gilvânia B. Cavalcante; Maria Rose Jane R. Albuquerque

The chemical composition of the essential oils, obtained by hidrodistillation, from leaves of two Vernonia species (V. remotiflora and V. brasiliana), was determined by GC-FID and GC-MS. Both essential oils were predominantly constituted by sesquiterpenes (92.0 - 93.4%). The main constituents of the oil from V. brasilana were (E)-caryophyllene (36.7%), germacrene D (35.5%), and α-humulene (11.7%), while (E)-caryophyllene (42.2%) and bicyclogermacrene (20.0%) were the major ones in the oil from V. remotiflora. Although with moderate activity both oils showed acetylcholinesterase and antibacterial activities.


BioMed Research International | 2014

Antimicrobial Effect of the Triterpene 3β,6β,16β-Trihydroxylup-20(29)-ene on Planktonic Cells and Biofilms from Gram Positive and Gram Negative Bacteria

Francisco Flávio Vasconcelos Evaristo; Maria Rose Jane R. Albuquerque; Hélcio Silva dos Santos; Paulo Nogueira Bandeira; Fábio Nascimento Ávila; Bruno Rocha da Silva; Ariana Azevedo Vasconcelos; Érica de Menezes Rabelo; Luiz Gonzaga do Nascimento-Neto; Francisco Vassiliepe Sousa Arruda; Mayron Alves de Vasconcelos; Victor Alves Carneiro; Benildo Sousa Cavada; Edson Holanda Teixeira

This study evaluated the antimicrobial effect of 3β,6β,16β-trihydroxylup-20(29)-ene (CLF1), a triterpene isolated from Combretum leprosum Mart., in inhibiting the planktonic growth and biofilms of Gram positive bacteria Streptococcus mutans and S. mitis. The antimicrobial activity was assessed by determining the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). The antibiofilm potential was determined by quantifying total biomass and enumerating biofilm-entrapped viable bacteria. In addition, the acute toxicity of CLF1 on Artemia sp. nauplii was also determined. The results showed that CLF1 was able in inhibiting the growth of S. mutans and S. mitis with MIC and MBC of 7.8 μg/mL and 15.6 μg/mL, respectively. CLF1 was highly effective on biofilms of both bacteria. Only 7.8 μg/mL CLF1 was enough to inhibit by 97% and 90% biomass production of S. mutans and S. mitis, respectively. On the other hand, such effects were not evident on Gram negative Pseudomonas aeruginosa and Klebsiella oxytoca. The toxicity tests showed that the LC50 of CLF1 was 98.19 μg/mL. Therefore, CLF1 isolated from C. leprosum may constitute an important natural agent for the development of new therapies for caries and other infectious diseases caused by S. mutans and S. mitis.


Journal of Essential Oil Research | 2001

Volatile Constituentes from Leaves of Vernonia chalybaea Mart. and Eupatorium ballotaefolium H.B.K.

Maria Rose Jane R. Albuquerque; Elnatan Bezerra de Souza; Elenice F. Mesquita; Edson Paula Nunes; Adriano N. Cunha; Edilberto R. Silveira

Abstract The essential oils from leaves of Vernonia chalybaea and Eupatorium ballotaefolium were analyzed by GC/MS. The oil obtained from V. chalybaea was characterized by the presence of β-pinene (30.6%), β-caryophyllene (12.1%), whereas the oil of E. ballotaefolium was characterized by limonene (15.3%) and (E)-β-ocimene (10.5%) as the major constituents.


BioMed Research International | 2014

Antibacterial and antioxidant activities of Derriobtusone A isolated from Lonchocarpus obtusus

Mayron Alves de Vasconcelos; Francisco Vassiliepe Sousa Arruda; Daniel Barroso de Alencar; Silvana Saker-Sampaio; Maria Rose Jane R. Albuquerque; Hélcio Silva dos Santos; Paulo Nogueira Bandeira; Otília Deusdênia L. Pessoa; Benildo Sousa Cavada; Mariana Henriques; Maria Olívia Pereira; Edson Holanda Teixeira

This study evaluated the effect of derriobtusone A, a flavonoid isolated from Lonchocarpus obtusus, on two important pathogenic bacteria, Staphylococcus aureus and Escherichia coli, as well as its antioxidant activity and toxicity. Planktonic growth assays were performed, and the inhibition of biofilm formation was evaluated. In addition, antioxidant activity was assessed by DPPH radical scavenging assay, ferrous ion chelating assay, ferric-reducing antioxidant power assay, and β-carotene bleaching assay. Toxicity was evaluated by the brine shrimp lethality test. Results showed that derriobtusone A completely inhibited the planktonic growth of S. aureus at 250 and 500 μg/mL; however, it did not have the same activity on E. coli. Derriobtusone A reduced the biomass and colony-forming unit (cfu) of S. aureus biofilm at concentrations of 250 and 500 μg/mL. In various concentrations, it reduced the biofilm biomass of E. coli, and, in all concentrations, it weakly reduced the cfu. Derriobtusone A showed highly efficient antioxidant ability in scavenging DPPH radical and inhibiting β-carotene oxidation. The compound showed no lethality to Artemia sp. nauplii. In conclusion, derriobtusone A may be an effective molecule against S. aureus and its biofilm, as well as a potential antioxidant compound with no toxicity.


Química Nova | 2013

Constituintes químicos de Vernonia scorpioides (Lam) Pers. (Asteraceae)

Adalva Lopes Machado; Fabiana Martins Aragão; Paulo Nogueira Bandeira; Hélcio Silva dos Santos; Maria Rose Jane R. Albuquerque; Otília Deusdênia L. Pessoa; Edilberto R. Silveira; Edson Paula Nunes; Raimundo Braz-Filho

CHEMICAL CONSTITUENTS OF Vernonia scorpioides (Lam) Pers. (Asteraceae). The chemical investigation of hexane and ethanol extracts from the aerial parts of Vernonia scorpioides resulted in the isolation and characterization of a new polyacetylene lactone, rel-4-dihydro-4β-hydroxy-5a-octa-2,4,6-triynyl-furan-2-(5H)-one, along with the new ethyl 3,4-dihydroxy-6,8,10-triynyldodecanoate, and seven known compounds: taraxasteryl acetate, lupeyl acetate, lupeol, lupenone, β-sitosterol, stigmasterol and luteolin. The structure of all compounds was determined by spectrometric techniques (HR-ESI-MS, 1H and 13C NMR and IV) and comparison with published spectral data.

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Raimundo Braz-Filho

Universidade Federal Rural do Rio de Janeiro

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Telma L. G. Lemos

Federal University of Ceará

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