36 research outputs found

    Molecular identification of three Habenaria species from Binh Chau-Phuoc Buu Nature Reserve, Vietnam

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    The present provides molecular data for species of Habenaria diphylla (Nimmo) Dalzell, H. khasiana Hook.f. and H. rostellifera Rchb.f. collected from Binh Chau-Phuoc Buu Nature Reserve, Vietnam for the first time. Along with other DNA sequences from GenBank database, the phylogenetic trees for Habenaria species from Vietnam have been established

    Chemical Components of Essential Oils From the Leaves of Seven Species Belonging to Rutaceae Family from Binh Chau-Phuoc Buu Nature Reserve, Vietnam

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    Several plant species of the Rutaceae family are medicinal plants, oil bearing and food crops. To provide more information for utilization of some species of this family in Binh Chau-Phuoc Buu Nature Reserve, we extracted essential oils from the leaves of seven species of the Rutaceae family: Acronychia pedunculata (L.) Miq., Atalantia citroides Pierre ex Guillaumin, Clausena excavata Burm.f., Glycosmis pentaphylla (Retz.) DC., Luvunga scandens (Roxb.) Buch.-Ham. ex Wight & Arn, Melicope pteleifolia (Champ. ex Benth.) T.G. Hartley, and Micromelum sp., via hydrodistillation, and identified their components using GC/MS analysis. A total of 60 compounds were identified from essential oils of seven species. The main components of the essential oils isolated from five species, including A. pedunculata, C. excavata, M. pteleifolia, G. pentaphylla, and Micromelum sp., were caryophyllene (57.63% and 55.41% in A. pedunculata and C. excavata, respectively), 1,9-decadiyne (32.59%, M. pteleifolia), β-ocimene (23.10%, G. pentaphylla), and 3-carene (58.03%, Micromelum sp.). Additionally, this study revealed the chemical composition of essential oils of L. scandens and A. citroides for the first time. The main constituent of A. citroides was 7-oxabicyclo[4.1.0] heptane, 3-oxiranyl- (53.91%) and that of L. scandens was caryophyllene (34.66%). These findings provide the basis for further application of these species in medicine

    Rifampicin resistant 'Mycobacterium tuberculosis' in Vietnam, 2020–2022

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    Objective: We conducted a descriptive analysis of multi-drug resistant tuberculosis (MDR-TB) in Vietnam’s two largest cities, Hanoi and Ho Chi Minh city. Methods: All patients with rifampicin resistant tuberculosis were recruited from Hanoi and surrounding provinces between 2020 and 2022. Additional patients were recruited from Ho Chi Minh city over the same time period. Demographic data were recorded from all patients, and samples collected, cultured, whole genome sequenced and analysed for drug resistance mutations. Genomic susceptibility predictions were made on the basis of the World Health Organization’s catalogue of mutations in Mycobacterium tuberculosis associated with drug resistance, version 2. Comparisons were made against phenotypic drug susceptibility test results where these were available. Multivariable logistic regression was used to assess risk factors for previous episodes of tuberculosis. Results: 233/265 sequenced isolates were of sufficient quality for analysis, 146 (63 %) from Ho Chi Minh City and 87 (37 %) from Hanoi. 198 (85 %) were lineage 2, 20 (9 %) were lineage 4, and 15 (6 %) were lineage 1. 17/211 (8 %) for whom HIV status was known were infected, and 109/214 (51 %) patients had had a previous episode of tuberculosis. The main risk factor for a previous episode was HIV infection (odds ratio 5.1 (95 % confidence interval 1.3–20.0); p = 0.021). Sensitivity for predicting first-line drug resistance from whole genome sequencing data was over 90 %, with the exception of pyrazinamide (85 %). For moxifloxacin and amikacin it was 50 % or less. Among rifampicin-resistant isolates, prevalence of resistance to each non-first-line drug was < 20 %. Conclusions: Drug resistance among most MDR-TB strains in Vietnam’s two largest cities is confined largely to first-line drugs. Living with HIV is the main risk factor among patients with MDR-TB for having had a previous episode of tuberculosis

    Pharmacists’ Perspectives on the Use of Telepharmacy in Response to COVID-19 Pandemic in Ho Chi Minh City, Vietnam

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    Introduction: Telepharmacy, the application of information and communication technologies in healthcare services, has been adopted in many countries to provide patients with pharmaceutical care. However, it has yet to be widely used in Vietnam. This study was conducted to assess the current status of use and the factors associated with the willingness to use telepharmacy of pharmacists in Vietnam. Methods: A descriptive cross-sectional study was conducted from February to July 2021; 414 pharmacists were recruited to fill in an online survey. Results: Overall, 86.7% of participants have used telepharmacy application and 87.2% of them were willing to apply telepharmacy in pharmacy practice. According to our multivariate analysis, the level of readiness was associated with positive attitude (odds ratio [OR] = 4.67; 95% confidence interval [CI]: 2.26-9.66), and a good behavior (OR = 11.34; 95% CI: 3.84-33.45). Discussion: Developing a telepharmacy system with appropriate features is essential to meet the requirements of pharmacy practice amid the spread of the COVID-19 pandemic

    Loeseneriella A. C. Sm.

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    8. Loeseneriella A.C.Sm. 1(52) Loeseneriella chesseana (Pierre) Tardieu 2(53) Loeseneriella dinhensis (Pierre) A.C.Sm. 3(54) Loeseneriella merrilliana A.C.Sm. (Tardieu-Blot 1948b, Nguyen 2003a) 4(55) Loeseneriella pauciflora (DC.) A.C.Sm. (Nguyen 2003a, Pham 2003)Published as part of Pham, Ngoc Hoai, Ren, Ming-Xun, Nuraliev, Maxim S., Trinh, Ngoc Bon, Nguyen, Tien Dat, Ragupathi, Gopi & Pham, Van The, 2022, The genus Parnassia in Vietnam, and a checklist of Vietnamese Celastraceae, pp. 213-227 in Phytotaxa 536 (3) on page 226, DOI: 10.11646/phytotaxa.536.3.2, http://zenodo.org/record/633184

    Glyptopetalum Thwaites

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    6. Glyptopetalum Thwaites 1(31) Glyptopetalum annamense Tardieu 2(32) Glyptopetalum calyptratum Pierre 3(33) Glyptopetalum chaudocense Pierre 4(34) Glyptopetalum gracilipes Pierre (Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 5(35) Glyptopetalum harmandianum Pierre (Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 6(36) Glyptopetalum integrifolium Q.W.Lin, Z.X.Zhang & Q.R.Liu 7(37) Glyptopetalum longepedunculatum Tardieu 8(38) Glyptopetalum poilanei Tardieu 9(39) Glyptopetalum quadrangulare Prain ex King (Savinov 2014) 10(40) Glyptopetalum sclerocarpum (Kurz) M.A.Lawson (Hoang 2008, Pham 2003, Savinov et al. 2018) 11(41) Glyptopetalum thorelii Pit. (Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 12(42) Glyptopetalum tonkinense Pit.Published as part of Pham, Ngoc Hoai, Ren, Ming-Xun, Nuraliev, Maxim S., Trinh, Ngoc Bon, Nguyen, Tien Dat, Ragupathi, Gopi & Pham, Van The, 2022, The genus Parnassia in Vietnam, and a checklist of Vietnamese Celastraceae, pp. 213-227 in Phytotaxa 536 (3) on pages 225-226, DOI: 10.11646/phytotaxa.536.3.2, http://zenodo.org/record/633184

    Celastrus L.

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    3. Celastrus L. 1(3) Celastrus annamensis Tardieu 2(4) Celastrus gemmatus Loes. (Merrill 1938, Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 3(5) Celastrus glaucophyllus Rehder & E.H.Wilson (Hou 1955) 4(6) Celastrus hindsii Benth. (Pitard 1912a, Tardieu-Blot 1948a, Hou 1955, Nguyen 2003a, Pham 2003) 5(7) Celastrus hirsutus Comber (Hou 1955) 6(8) Celastrus hookeri Prain (Merrill 1938, Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 7(9) Celastrus monospermus Roxb. (Merrill 1938, Tardieu-Blot 1948a, Hou 1955, Nguyen 2003a, Pham 2003) 8(10) Celastrus orbiculatus Thunb. (Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 9(11) Celastrus paniculatus Willd. (Pitard 1912a, Tardieu-Blot 1948a, Hou 1955, Nguyen 2003a, Pham 2003) 10(12) Celastrus rosthornianus Loes. (Merrill 1938, Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 11(13) Celastrus stylosus Wall. (Hou 1955)Published as part of Pham, Ngoc Hoai, Ren, Ming-Xun, Nuraliev, Maxim S., Trinh, Ngoc Bon, Nguyen, Tien Dat, Ragupathi, Gopi & Pham, Van The, 2022, The genus Parnassia in Vietnam, and a checklist of Vietnamese Celastraceae, pp. 213-227 in Phytotaxa 536 (3) on page 225, DOI: 10.11646/phytotaxa.536.3.2, http://zenodo.org/record/633184

    Gymnosporia Benth. & Hook.

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    7. Gymnosporia (Wight & Arn.) Benth. & Hook. f. 1(43) Gymnosporia bonii Pit. 2(44) Gymnosporia chevalieri Tardieu 3(45) Gymnosporia crassifolia Pit. 4(46) Gymnosporia diversifolia Maxim. (Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 5(47) Gymnosporia marcanii Craib (Tardieu-Blot 1948a, Nguyen 2003a, Pham 2003) 6(48) Gymnosporia mekongensis Pierre 7(49) Gymnosporia stylosa Pierre 8(50) Gymnosporia tonkinensis Pit. 9(51) Gymnosporia wallichiana (Spreng.) M.A.Lawson (Pitard 1912a, Tardieu-Blot 1948a, Nguyen 2003a)Published as part of Pham, Ngoc Hoai, Ren, Ming-Xun, Nuraliev, Maxim S., Trinh, Ngoc Bon, Nguyen, Tien Dat, Ragupathi, Gopi & Pham, Van The, 2022, The genus Parnassia in Vietnam, and a checklist of Vietnamese Celastraceae, pp. 213-227 in Phytotaxa 536 (3) on page 226, DOI: 10.11646/phytotaxa.536.3.2, http://zenodo.org/record/633184

    Plagiopteron Griff.

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    12. Plagiopteron Griff. 1(72) Plagiopteron suaveolens Griff. (Chinh et al. 2016, Nghiem et al. 2017)Published as part of Pham, Ngoc Hoai, Ren, Ming-Xun, Nuraliev, Maxim S., Trinh, Ngoc Bon, Nguyen, Tien Dat, Ragupathi, Gopi & Pham, Van The, 2022, The genus Parnassia in Vietnam, and a checklist of Vietnamese Celastraceae, pp. 213-227 in Phytotaxa 536 (3) on page 226, DOI: 10.11646/phytotaxa.536.3.2, http://zenodo.org/record/633184
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