Academic literature on the topic 'Hibiscus sabdariffa'
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Journal articles on the topic "Hibiscus sabdariffa"
Kwofie, J., H. M. Amoatey, W. Nunekpeku, J. K. Ahiakpa, and C. Katsepor. "Crossability Studies among Twenty Accessions of Roselle (Hibiscus sabdariffa L.)." Journal of Agricultural Science 9, no. 9 (August 15, 2017): 230. http://dx.doi.org/10.5539/jas.v9n9p230.
Full textBarros de Nogueira, Ruama Viana, Virginia Freitas Rodrigues, Sílvia Menezes de Faria Pereira, and Inêz Barcellos de Andrade. "FLORES DE HIBISCO (Hibiscus sabdariffa) COMERCIALIZADAS NO MUNICÍPIO DE CAMPOS DOS GOYTACAZES-RJ: UMA ANÁLISE DO PERFIL FITOQUÍMICO E DO USO POPULAR, CONSIDERANDO ATIVIDADES ATRIBUIDAS ÀS RESPECTIVAS CLASSES DE METABÓLIDOS SECUNDÁRIOS ENCONTRADAS." Revista Científica da Faculdade de Medicina de Campos 16, no. 1 (April 30, 2021): 12–18. http://dx.doi.org/10.29184/1980-7813.rcfmc.253.vol.16.n1.2021.
Full textKarmana, I. Wayan. "Artikel Review : Bioaktivitas Bunga Rosella (Hibiscus sabdariffa L.) Beserta Pemanfaatannya." Educatoria : Jurnal Ilmiah Ilmu Pendidikan 3, no. 3 (July 30, 2023): 208–16. http://dx.doi.org/10.36312/educatoria.v3i3.200.
Full textYuliastri, W. O., A. Diantini, M. Ghozali, I. Sahidin, and M. Isrul. "PHYTOCHEMICAL CONSTITUENT AND In-vitro CYTOTOXIC ACTIVITY OF Hibiscus sabdariffa L. CALYX FRACTION ON HUMAN BREAST CANCER CELL LINE MDA-MB-231." RASAYAN Journal of Chemistry 15, no. 03 (2022): 1619–25. http://dx.doi.org/10.31788/rjc.2022.1536694.
Full textLestari, Gusti Ayu Dewi. "SKRINING FITOKIMIA DAN UJI AKTIVITAS ANTIOKSIDAN EKSTRAK ETANOL BUNGA ROSELLA UNGU (Hibiscus sabdariffa L.)." Jambura Journal of Chemistry 4, no. 1 (March 10, 2022): 17–24. http://dx.doi.org/10.34312/jambchem.v4i1.11157.
Full textKasimo, Elfred, Lisa Savitri, Mujtahid Bin Abd Kadir, Moh Alimansur, and Ester Lianawati Antoro. "TOKSISITAS KOMBINASI EKSTRAK ROSELA (Hibiscus sabdariffa L.) DAN PARE (Momordica charantia) DENGAN METODE BRINE SHRIMP LETHALITY TEST (BSLT)." GEMA KESEHATAN 15, no. 2 (December 28, 2023): 168–76. http://dx.doi.org/10.47539/gk.v15i2.441.
Full textFirmasari, Firmasari, Ni Ketut Sumarni, Ruslan, and Hardi Ys. "PERSEN DEGRADASI EKSTRAK ETANOL KELOPAK BUNGA ROSELLA (Hibiscus sabdariffa L.) SELAMA PENYIMPANAN THE PERCENTAGE OF ETHANOL EXTRACTS OF ROSELLE PETALS (Hibiscus sabdariffa L.) DURING STORAGE." KOVALEN: Jurnal Riset Kimia 5, no. 2 (August 31, 2019): 132–38. http://dx.doi.org/10.22487/kovalen.2019.v5.i2.9970.
Full textChoon Yoong Cheok and Anusuyah Ragunathan. "Anthocyanin degradation kinetics and thermodynamic analysis of Hibiscus rosa-sinensis L. Clitoria ternatea L. and Hibiscus sabdariffa L." Progress in Energy and Environment 19, no. 1 (August 23, 2022): 1–12. http://dx.doi.org/10.37934/progee.19.1.112.
Full textFreitas, Nélio Martins, Angela Maria Correa Mouzinho Santos, and Lucy Rose de Maria Oliveira Moreira. "AVALIAÇÃO FITOQUÍMICA E DETERMINAÇÃO DE MINERAIS EM AMOSTRAS de Hibiscus sabdariffa L (vinagreira)." Cadernos de Pesquisa 20, no. 3 (December 21, 2013): 65. http://dx.doi.org/10.18764/2178-2229.v20n3p65-72.
Full textKazi, Atik Mubarak, and Ramasastry DVA. "Characterization of continuous Hibiscus sabdariffa fibre reinforced epoxy composites." Polymers and Polymer Composites 30 (January 2022): 096739112110609. http://dx.doi.org/10.1177/09673911211060957.
Full textDissertations / Theses on the topic "Hibiscus sabdariffa"
Paul, Hélène. ""Hibiscus sabdariffa" L." Paris 5, 1995. http://www.theses.fr/1995PA05P111.
Full textSindi, Hebah Abbas. "Bioactivity of anthocyanins from Hibiscus sabdariffa." Thesis, University of Leeds, 2013. http://etheses.whiterose.ac.uk/5910/.
Full textSie, Raoul Sylvère. "Caractérisation agro-morphophysiologique et micropropagation de l’oseille de Guinée (Hibiscus Sabdariffa L. )." Brest, 2010. http://www.theses.fr/2010BRES2014.
Full textRoselle (Hibiscus sabdariffa L. ) is an important crop in West Africa for its nutritional, industrial and medicinal uses. However, except some studies on phytotechny, there are a few report on the selection of this plant. Moreover, no study on thie in vitro regeneration by somatic embryogenesis is available. The main aim of this work is to characterize the collection of roselle for in long-term sight, to implement a programme of selection for vigorous, high yielding and resistant genotypes te certain diseases. Moreover, die conservation ami seeds production ofgood genotypes, require the development of methods of regeneration by in vitro culture. The first part of the study relating to the morphological and agronomical characterization of the collection of roselle, confirmed the organization of this species into two varieties such as sabdariffa and altissima whose phenotypes were complementary. H. Sabdariffa var. Sabdariffa was characterized by a strong early vegetative vigour, a low yielding of calyx and fruits, a low photoperiod susceptibility and a red color of plants. H. Sabdariffa var. Altissima had a strong adult vegetative vigour, a higher yielding, a high photoperiod susceptibility and a green color of the plant. In a second part, the varieties were evaluated for their defense reactions against to pathogenic fungi (Fusarium oxysporum and Phoma sabdariffae). Studies ou the impact of the attacks on the growth of the plants and certain physiological parameters, showed that the individuals of the sabdariffa variety were more resistaut to both fungi than those of the altissima variety. No incidence was observed on both varieties photosynthesis. Following die inoculations, the sabdariffa variety accumulated an increasing quantity of polyphenols but this rate decreases in the altissima variety. The last part describes the methods used to induce the formation of embryogenic calli, preceded by the development of an efficient protocol of decontamination of explants. The technique of the thin Transversal Cell Layers (tTCLs) implemented on seedlings, enabled to obtain some embryogenic calli after the study of many determining factors such as the genotype (sabdariffa, altissima), the culture medium (MS, DKW), the nature of the explant (root, hypocotyle, cotyledon), the type (auxines, cytokinines) and the content of the growth regulaters. The tTCLs from hypocotyl and cotyledon in culture medium DKW containing combinations 1/0,5 (mg/l) and 4/1 (mg/l) of 2,4-D/TDZ constituted the best conditions of induction of the embryogenic calli
Sinela, André Mundombe. "Etude des mécanismes réactionnels et des cinétiques de dégradation des anthocyanes dans un extrait d’Hibiscus sabdariffa L." Thesis, Montpellier, SupAgro, 2016. http://www.theses.fr/2016NSAM0036/document.
Full textDried calyx of Hibiscus sabdariffa L. are traditionally used in Africa for beverage production by maceration in water. This raw material, rich in anthocyanins, is also known in the food industry as a source of natural dyes. However, the color of extracts obtained quickly changes over time which affects the development of these products. To better characterize and understand the instability of color, this work provides a mechanistic and kinetic study of the degradation of anthocyanins during the conservation of an extract from H. sabdariffa. Biochemical characterization of the extract allowed to identify predominant polyphenols (delphinidin 3-O-sambubioside Del-3Sb, cyanidin 3-O-sambubioside Cya-3Sb and caffeoylquinic acids) and highlighted the presence of metals known as potential oxidation catalysts (Fe, Cu, Mn). Kinetics of degradation of anthocyanins in the extract were followed by HPLC-DAD between 4 and 37 ° C for 60 days. It can be represented by a first order model. Del-3Sb (Ea = 90 kJ mol-1) is more sensitive to temperature increase than Cya-3Sb (Ea = 80 kJ.mol-1). Influence of different factors on the degradation of anthocyanins was studied in simplified model media. Rate constant of degradation (k) of Del-3Sb on model media containing Fe (III), Cu (II) and Mn (II) at similar concentrations to those of the extract was similar to that measured in the extract. For Cya-3Sb it was 40% lower than in the extract. Increasing Fe concentration of 1 to 13 mg.L 1 increased by about 3-fold the k of anthocyanins. Adding chlorogenic acid in a model media containing Fe increased k of Cya-3Sb 42%. Opposite effect was observed for Del-3Sb (47% decrease). Dissolved oxygen content has no influence on k of anthocyanins. Two mechanisms of degradation of anthocyanins have been identified: the scission mechanism, representing a minority pathway (10% of degraded anthocyanins) with production of phloroglucinaldehyde, gallic acid (from Del-3Sb) and protocatechuic (from Cya -3Sb). The other mechanism is condensation with formation of brown polymers, it is promoted by increasing of concentration of Fe was and mixture of Fe, Cu and Mn. Conclusions led to perspectives on study of impact of other compound in the extract (sugar, amino-acids) as well as identification and quantification of brown polymers
MALACRIDA, ALESSIO. "EVALUATION OF ANTITUMORAL EFFECTS OF HIBISCUS SABDARIFFA ON MULTIPLE MYELOMA CELLS." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2017. http://hdl.handle.net/10281/158152.
Full textHibiscus Sabdariffa (HS) is a plant of the Malvacee family commonly cultured in tropical and subtropical countries. It is mainly known as the main ingredient for the preparation of cold drink called Karkadè. Calices and leaves of HS plant are also used in folk medicine thanks to their antioxidant and anti-inflammatory properties. In recent years, HS has also gained great interest as a possible antitumoral agent. In the present PhD project, we evaluated the antitumoral effects of HS against multiple mye-loma cells in vitro. Multiple myeloma is the most frequent hematological malignancy world-wide. In recent years, new drugs have increased the survival expectancy of patients. Despite this, new therapeutic approaches are necessary, especially for high multiple myeloma hetero-geneity and for relapsed or refractory multiple myeloma. The project was organized in three distinct phases: 1- Evaluation of antitumoral effects of HS against RPMI 8226 human multiple myeloma cells. We demonstrated by MTT and Trypan blue assays that a total HS extract (HSE) and one of its fraction obtained by liquid-liquid extraction (HSEC) were able to impair cell viability of human multiple myeloma RPMI 8226 in a dose and time dependent manner. HSE cell viability reduction was due to a cytostatic action, while HSEC was more cytotoxic and induced a caspase dependent apoptosis. Moreover, both HSE and HSEC impaired cell migration and invasion of RPMI 8226 cells in a Boyden chamber as-say. We also demonstrated in in vitro model of neurotoxicity (dorsal root ganglia model) that HSE and HSEC concentrations used in our experiments were not neurotoxic. In RPMI 8226 cells autophagy and proteasome activity were impaired by both HSE and HSEC. MAPK p38 activation was observed in the first 6h of treatment, while ERK 1 and ERK 2 activation occurred between 16 and 48h. 2- Evaluation of combinations between Bortezomib (BTZ) and HSE or HSEC against RPMI 8226 multiple myeloma cells. We evaluated several combinations between BTZ and HSE or HSEC (simultaneous, not-simultaneous treatment and pretreatment) using MTT assay to assess their effectiveness. Among all evaluated combinations, only the 24h BTZ 1nM pretreatment followed by HSE or HSEC treatment resulted more effective than BTZ or HSE or HSEC single treatment in reducing cell viability. This combination was not neurotoxic in the dorsal root ganglia model. 3- Isolation and characterization of HSEC molecules responsible of the antitumoral ef-fect. Using a bioguided method, we isolated several fractions from HSEC. Fractions were obtained by flash column chromatography or by resin use. Molecular characterization was performed by HPLC, NMR or mass spectrometry, while biological activity was screened in human multiple myeloma RPMI 8226 cells by MTT and proteasome activity assay. We isolated three fractions with a first fractionating process that keep their activ-ity on RPMI 8226 cells, but that are not completely pure. In a second fractionating, we isolated a highly pure fraction with a significant activity on RPMI 8226 cell viability. We also characterized this fraction by both a molecular and biological point of view. In conclusion, we demonstrated the antitumoral effect of HS in vitro against RPMI 8226 multiple myeloma cells. We also found a new therapeutic combination between BTZ and HS that enhanced their antitumoral effect when compared to single treatments. Moreover, we also isolated one of the molecules that are involved in the antitumoral effect of HS. The results of my PhD project showed that HS could be a promising chemotherapeutic agent, but further studies are still needed.
Omoarukhe, Esereosa D. "Natural processing for beverages : from a Hibiscus sabdariffa (Roselle) beverage perspective." Thesis, University of Reading, 2017. http://centaur.reading.ac.uk/78761/.
Full textMaciel, Mônica Jachetti. "Avaliação do extrato alcoólico de hibisco (hibiscus sabdariffa l.) como fator de proteção antibacteriana e antioxidante em alimentos." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2011. http://hdl.handle.net/10183/29544.
Full textThe hibiscus (Hibiscus sabdariffa L.) has antioxidant and antimicrobial properties and it is utilized as functional food and medicinal plant in tropical countries. Through of Dilution Testing in Multiple Tubes System, it were determined the intensity of bacterial inhibition activity (IINIB/ Bacteriostasy) and the intensity of bacterial inactivation activity (IINAB/ Bactericidie) of alcoholic extracts of two accesses of hibiscus, known as: Palmares do Sul/RS and Porto Alegre/RS on standardized inoculum of Enterococcus faecalis (ATCC 19433), Escherichia coli (ATCC 11229), Salmonella Enteritidis (ATCC 11076) and Staphylococcus aureus (ATCC 25923). At the same time, the total content of polyphenols and anthocyanins in the calyxes and fruits with seeds hibiscus was determined. The antimicrobial activity of alcoholic extract of the calyxes in both accesses showed a significant positive difference when related to the alcoholic extract of the fruits with seeds. Salmonella enteritidis was the most sensitive bacteria to the alcoholic extract of calyxes of the hibiscus while the most resistant was Staphylococcus aureus, independent of the variable access, considering only the plant structure. In relation to the alcoholic extract of the fruits with seeds, Escherichia coli showed the highest sensitivity and Staphylococcus aureus the highest resistence. Total polyphenols and anthocyanins of alcoholic extract of calyxes‟s values showed a significant difference and they were superior to alcohol extract of fruits with seeds. Possibly there is a direct relationship between the concentration of anthocyanin and antibacterial activity in different structures of the hibiscus plant.
Piovesana, Alessandra. "Extração, identificação, quantificação e microencapsulamento por atomização e liofilização de compostos bioativos dos cálices de hibisco (hibiscus sabdariffa l.)." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2016. http://hdl.handle.net/10183/151290.
Full textThe interest in the extraction of bioactive compounds from natural sources, for use in the production of functional foods has increased, mainly due to the growing demand by consumers for healthier products and can bring health benefits. Among the natural sources of bioactive compounds, stands out the hibiscus (Hibiscus sabdariffa L.), which is rich in anthocyanins, flavonoids, phenolic acids, carotenoids, among others. However, when the bioactive compounds are separated from their matrix, they become highly unstable against various environmental factors and need to be protected. The coating by microencapsulation is an alternative to slow the degradation of these compounds. This study aimed at the extraction, identification, quantification and microencapsulation by spray drying and freeze drying of bioactive compounds of hibiscus calyces. Firstly, a thorough exhaustive extraction of carotenoids and phenolic compounds by organic solvents was performed for identification and quantification of these compounds. The extraction of anthocyanins was also studied along with other phenolic compounds by an aqueous solvent acidified (2% citric acid, w/v). From the best treatment for extraction, the extract obtained was microencapsulated by spray drying and freeze drying using Arabic gum (GA), partially hydrolyzed guar gum (PHGG) and polydextrose (PD) as encapsulating agents in a concentration of 10%. Carotenoids and phenolic compounds were identified and quantified by HPLC-DAD-MS/MS (high-performance liquid chromatography with diode array detection and mass spectrometry). Twenty-one carotenoids were found, of which fifteen were identified. The total carotenoids in hibiscus calyces was 641.38 ± 23.61 mg/100 g fresh weight, with the all-trans-lutein and all-trans-β-carotene the major compounds, representing 49 and 23%, respectively. Regarding the phenolic compounds it was found twenty of those, of which fourteen have been identified. Anthocyanins were the main components in the hibiscus calyces, and delphinidin and cyanidin 3-sambubioside 3-sambubioside represented 41 and 13% of total phenolic compounds, respectively. Among the phenolic acids, the major components were the 3-caffeoylquinic acid and 5-caffeoylquinic acid, representing 15 and 13% of total phenolic compounds, respectively. For acidified aqueous extraction, we used a fractional factorial design (24-1) with four factors: enzyme concentration, temperature, stirring speed and extraction time. From the ANOVA, the main and interaction effects were assessed as answers: Chroma, total anthocyanins monomeric (TMA), reducing capacity, ABTS and phenolic compounds. From the results, the best treatment was with 55 °C, 50 μL of enzyme/1000 g extract, 400 rpm and 4 hours of extraction, it was obtained in this extraction condition 3.82 mg/g extract on a dry basis for TMA and 17.59 mg/g extract on a dry basis for phenolic compounds, which resulted in antioxidant capacity of 7.72 μmol Eq. Trolox/g extract on a dry basis, evaluated by ABTS and 3.96 mg GAE/g extract on a dry basis, assessed by reducing capacity. This extract was used for the encapsulation study, by spray drying (140 °C) and freeze drying (-68 ° C for 24 hours) using GA, PHGG, and PD as encapsulants. It was observed that the best treatment is by freeze drying using GA as encapsulant, resulting in 2.83 mg/g sample on dry basis for TMA, antioxidant capacity of 2.98 mg GAE/g sample on dry basis and 5.67 μmol Eq. Trolox/g sample on dry basis, evaluated by reducing capacity and ABTS, respectively. However, when we evaluated the physical and morphological properties of powders, samples prepared by spray drying and using GA and PHGG showed the best performance, and the values for solubility, hygroscopicity and moisture were 95.8 and 95.2%, 31.3 and 28.9%, 1.9 and 2.4%, respectively. For the glass transition temperature (Tg), treatments with GA and PHGG on both encapsulation methods had high Tg values ranging from 10.9 to 17.4 °C. As for treatments of PD as wall material, the values were (0.7 °C), both the spray drying as in freeze drying. In microscopy was also observed improved performance in spray-dried microparticles using GA and PHGG, which showed more spherical particles and with no tendency to attract and adhere to each other. Regarding the average particle diameter (D [4, 3]), the freeze-dried treatments had higher spray-dried particles ranging from 101.7 to 143.1 μm for freeze-dried, and 5.4 to 7.3 μm for spray-dried. As the span, which assesses particle size distribution ranged from 1.90 to 2.00 for spray-dried samples and 3.06 to 3.19 for the freeze-dried samples, indicating that there was a good uniformity in the size in the distribution of the size of the particle. It follows that hibiscus is a matrix with broad composition and bioactive compounds have potential for application in foods.
Cassol, Liliana. "Extração de compostos bioativos do hibisco (Hibiscus sabdariffa L.) por micro-ondas e seu encapsulamento por atomização e liofilização." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2018. http://hdl.handle.net/10183/179787.
Full textThe hibiscus calyces contend a high quantity of bioactive compounds responsible for their antioxidant activity. The present paper was aimed the production of extracts containing those bioactive compounds in acidified aqueous solution 2 % of citric acid by microwave assisted extraction (MAE) and the encapsulation of those extracts by spray drying and freeze-drying using polydextrose (PD), whey protein isolate (WPI) and their mixture in the concentration of 10 %. Previously three methods of extraction were studied, the first using only MAE at 200, 300 and 700 W of power, and times of 2, 5 and 8 minutes; the second consisted of two steps, the acid aqueous extraction with times of 1, 2, 4, 6, 18 and 24 hours followed by MAE at the powers of 200, 300 and 700 Watts; the third consisted of MAE followed by acid aqueous extraction, in the same times and powers mentioned for the second method. The results indicated that the best condition of the first method was 700 W and 8 minutes, the second method performed at 6 hours of acid aqueous extraction, followed by MAE at 700 W for 8 minutes and the third method, MAE at 700 W for 8 minutes followed by 6 hours of acid aqueous extraction. When the three methods are compared, the best condition of extraction was obtained in the third method: 1.63 mg delphinidin-3-sambubioside · g-1; 29.62 mg GAE · g-1; 133.25 μmol TE · g-1 for total monomeric anthocyanins, total phenolic compounds and antioxidant activity by ABTS, respectively. To evaluate the effect of the extraction obtained only by MAE, the extracts obtained by exhaustive extraction with methanol for 25 minutes and MAE at 700 W and 8 minutes were quantified by HPLC-DAD-ESI-MS/MS, was found 13 compounds (6 phenolic acids, 2 anthocyanins and 5 flavonoids derived from quercetin, kaempferol and myricetin). The phenolic compounds majorities were acid 3-caffeoylquinic (2.58 e 1.32 mg · g-1) and acid 5-caffeoylquinic (1.71 e 0.90 mg · g-1) for exhaustive extraction and MAE, respectively. That same extract (700 W and 8 minutes) was encapsulated by spray drying (160 ºC) and freeze-drying (- 68 °C for 54 hours). The obtained powders were evaluated about the levels of total phenolic compounds, total monomeric anthocyanins, antioxidant activity (ABTS, DPPH e HRSA), measured by spectrophotometric analysis, water activity, moisture, hygroscopicity, solubility, encapsulation efficiency, color, thermogravimetric analysis, glass transition temperature, Fourier transform infrared spectroscopy (FTIR) and microstructure (MEV). The spray dried powders had lower water activity (0.14 to 0.17), moisture (3.4 to 4.5 %), hygroscopicity (23.9 to 34.1 %), solubility (86 to 98.2 %) and encapsulation efficiency (51.62 to 84.52 %) than the freeze-dried powders. The results of FTIR showed that the encapsulants did not interact chemically, since changes were not observed on the frequency of the peaks; the thermogravimetric tests indicated that the powders presented the same tendency on the mass loss. On the microstructure analysis a better perform was observed on the spray dried microparticles with PD, which showed more spherical particles and with no tendency of attraction and adherence between them. Were obtained retentions of 38 to 77 % for total monomeric anthocyanins, 42 to 89 % for total phenolic compounds and between 33 and 90 % for antioxidant activity in the obtained powders. The encapsulated power by freeze-drying, with 10 % of polydextrose, was showed higher retention of anthocyanins (77 %), antioxidant activity by DDPH (90 %) and HRSA (74 %), however with higher hygroscopicity (39.4 %). The accelerated tests of storage (relative humidity of 75 and 90 % in temperatures of 40 and 60 ºC) performed in all the encapsulated powders, after 30 days, indicated that the freeze-drying treatment with 10 % of PD has the best behavior in those conditions, retaining 75 % of the phenolic compounds, with antioxidant activities measured by ABTS, DPPH and HRSA of 75, 90 and 74 %, respectively, present in the original extract. The obtained powder has potential for application in foods, therefore, due to the hibiscus being a matrix with ample composition of bioactive compounds.
Cissé, Mady. "Couplage de procédés membranaires pour la production d’extraits anthocyaniques : application à Hibiscus sabdariffa." Thesis, Montpellier, SupAgro, 2010. http://www.theses.fr/2010NSAM0035/document.
Full textHibiscus sabdariffa L. is a herbaceous plant, cultivated largely in tropical and subtropical areas of both hemispheres. In Senegal, where it was introduced in the 19th century, H. sabdariffa L. also called bissap or roselle is grown throughout the territory and operated primarily for its calyx. A refreshing drink is traditionally made from dried calyx by water extraction. The physical-chemical and biochemical characterization of the calyx allowed us to assess better the potential of this product. Thus, the calyx contained between 767 and 1480 mg.100g-1 of anthocyanins and between 1347 and 3736 mg.100g-1 of total polyphenols. They have an antioxidant capacity closed to 260 μmolTrolox.g-1. Malic acid is the major organic acid with content up to 2.3 g.100g-1. Because of these characteristics, the aqueous extract of H. sabdariffa calyx is an excellent source of anthocyanins. The work was then focused on the process for obtaining this extract. The study of solid-liquid extraction was performed from dried calyx with water at temperature range from 25 and 90 ° C. A maximum extraction yield of anthocyanin of 88 % was obtained at 25 ° C with a solid-to-solvent ratio of 1/25. Reducing the particle size and increasing the temperature decreased the extraction time but do not affect the extraction efficiency. A model of solid-liquid extraction which included the thermal anthocyanins degradation kinetics has been proposed and validated. Crossflow microfiltration with tubular ceramic 0.2 pore size membrane has produced a cold sterilized extract, stable during 90 days at 20 °C. We have shown here that the transmembrane pressure optimized at a volume reduction ratio (VRR) equal to 1 is no longer optimum when the VRR is increasing. To concentrate the anthocyanins present in the extract, the ultrafiltration membrane with a cutoff of 5 kDa can be used despite incomplete retention (95-97%). By cons, nanofiltration offers a tot al retention of anthocyanins. The method, implemented in semi-industrial conditions, has increased the content of total soluble solids (TSS) from 40 to 250 g.kg-1 at 35 °C at a transmembrane pressure between 20 and 30 bar with an average flow of 15 kg.h-1.m-2. The osmotic evaporation, tested on a pilot equipped with a polypropylene membrane of 10 m2, has concentrated anthocyanin extract up to 620 g TSS. kg-1. This concentrated extract retains all the physical-chemical, biochemical, nutritional and aromatic quality of the original extract. The evaporation flux is directly correlated with the total soluble solids content of the product to concentrate. Finally, various couplings of unit operations were compared to obtain a concentrated extract from H. sabdariffa calyx. The process which combines a cold extraction, a pre-concentration by nanofiltration and concentration by osmotic evaporation is the best way both in terms of investment costs and operating and quality of the ext ract
Books on the topic "Hibiscus sabdariffa"
Francisco de Jesús Caro Velarde, María Luisa Machuca Sánchez, Ericka Patricia Flores Berrios, and Francisco de Jesús Caro Velarde. El cultivo de jamaica en Nayarit: (Hibiscus sabdariffa L.). Tepic, Nayarit: Universidad Autónoma de Nayarit, 2012.
Find full textRoselle (Hibiscus sabdariffa). Elsevier, 2021. http://dx.doi.org/10.1016/c2019-0-04589-x.
Full textPadilla, Luis, Kamyre Neyra, Vladimir Huacasi, and Sonia Macedo. Efecto antibacterial in vitro del extracto etanolico de Hibiscus sabdariffa L. sobre cepas de Streptococcus mutans. Instituto Universitario de Innovación Ciencia y Tecnología Inudi Perú, 2022. http://dx.doi.org/10.35622/inudi.b.012.
Full textBook chapters on the topic "Hibiscus sabdariffa"
Ross, Ivan A. "Hibiscus sabdariffa." In Medicinal Plants of the World, 267–75. Totowa, NJ: Humana Press, 2003. http://dx.doi.org/10.1007/978-1-59259-365-1_13.
Full textLim, T. K. "Hibiscus sabdariffa." In Edible Medicinal and Non Medicinal Plants, 324–70. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-8748-2_23.
Full textBährle-Rapp, Marina. "Hibiscus sabdariffa." In Springer Lexikon Kosmetik und Körperpflege, 257. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_4746.
Full textKhare, C. P. "Hibiscus sabdariffa Linn." In Indian Medicinal Plants, 1. New York, NY: Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-70638-2_749.
Full textAzimova, Shakhnoza S., and Anna I. Glushenkova. "Hibiscus sabdariffa L." In Lipids, Lipophilic Components and Essential Oils from Plant Sources, 624. London: Springer London, 2012. http://dx.doi.org/10.1007/978-0-85729-323-7_2030.
Full textSastry, K. Subramanya, Bikash Mandal, John Hammond, S. W. Scott, and R. W. Briddon. "Hibiscus sabdariffa (Roselle) (Mesta)." In Encyclopedia of Plant Viruses and Viroids, 1167–68. New Delhi: Springer India, 2019. http://dx.doi.org/10.1007/978-81-322-3912-3_456.
Full textMojica, Luis, Li Rui, and Elvira Gonzalez de Mejia. "Hibiscus sabdariffa L.: Phytochemical Composition and Nutraceutical Properties." In ACS Symposium Series, 279–305. Washington, DC: American Chemical Society, 2012. http://dx.doi.org/10.1021/bk-2012-1109.ch017.
Full textVillani, Tom, H. Rodolfo Juliani, James E. Simon, and Qing-Li Wu. "Hibiscus sabdariffa: Phytochemistry, Quality Control, and Health Properties." In ACS Symposium Series, 209–30. Washington, DC: American Chemical Society, 2013. http://dx.doi.org/10.1021/bk-2013-1127.ch014.
Full textGonzález-Stuart, Armando. "Multifaceted Therapeutic Value of Roselle (Hibiscus sabdariffa L. – Malvaceae)." In Nutrients, Dietary Supplements, and Nutriceuticals, 215–26. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-308-4_14.
Full textTaşdemir, Munir, Çiğdem Gül, and Emine Dilara Kocak. "Use of Roselle (Hibiscus sabdariffa) in Composite Materials for Sustainability." In Sustainable Textiles: Production, Processing, Manufacturing & Chemistry, 97–115. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38013-7_5.
Full textConference papers on the topic "Hibiscus sabdariffa"
Gois, Camila Maria Dassie, Clara Beatriz de Lima, Daniela Cristina de Medeiros Araújo, and Jacqueline Godinho. "Avaliação da atividade antioxidante do extrato de Hibiscus sabdariffa in vitro." In II Congresso Internacional Interdisciplinar da Uningá. Editora Uningá, 2023. http://dx.doi.org/10.46311/ed.un.20221018116.
Full text"Tıbbi Bitki Hibiskus (Hibiscus sabdariffa L.)’un İn Vitro Çoğaltımı: Derleme." In PROCEEDING BOOK OF 1ST INTERNATIONAL CONFERENCE ON MODERN AND ADVANCED RESEARCH ICMAR 2023. All Sciences Academy, 2023. http://dx.doi.org/10.59287/icmar.1302.
Full textYani, Nadia Falihah Ahmad, Nurhazwani Ismail, and Kai Siang Oh. "Potential of using Hibiscus Sabdariffa in treating greywater." In PROCEEDINGS OF THE INTERNATIONAL ENGINEERING RESEARCH CONFERENCE - 12TH EURECA 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5120993.
Full textRithichai, P., Y. Jirakiattikul, C. Sriboonthai, and A. Itharat. "Bioactive Compounds and Antioxidant in Hibiscus sabdariffa Leaf." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608056.
Full textVinícius Falci and Caroline Maria Calliari. "Elaboração e caracterização de licor de Hibiscus sabdariffa." In XX Seminário de Iniciação Científica e Tecnológica da UTFPR. Curitiba, PR, Brasil: Universidade Tecnológica Federal do Paraná - UTFPR, 2015. http://dx.doi.org/10.20906/cps/sicite2015-0459.
Full textTrejo-Durán, M., E. Alvarado-Méndez, J. A. Andrade-Lucio, R. Rojas-Laguna, and M. A. Vázquez-Guevara. "Study of large nonlinear change phase in Hibiscus Sabdariffa." In SPIE Organic Photonics + Electronics, edited by Jon A. Schuller. SPIE, 2015. http://dx.doi.org/10.1117/12.2187562.
Full text"Moisture Dependent Aerodynamic Properties of Roselle Calyxes (Hibiscus Sabdariffa)." In 2015 NABEC Northeast Agr Bio Eng Conference. American Society of Agricultural and Biological Engineers, 2015. http://dx.doi.org/10.13031/nabec2015-042.
Full textGüler, Nilgün. "Staining effect of Hibiscus sabdariffa extract on Human Blood Cells." In 15th International Congress of Histochemistry and Cytochemistry. Istanbul: LookUs Scientific, 2017. http://dx.doi.org/10.5505/2017ichc.pp-71.
Full textAbdullah, B., S. Dhuha Khairunnisa, M. Iltizam Muhammad, and R. Sabrina Atwinda. "Isolation of anthocyanin from Indonesian purple roselle (Hibiscus sabdariffa L.) calyces." In PROCEEDINGS OF 2ND INTERNATIONAL CONFERENCE ON CHEMICAL PROCESS AND PRODUCT ENGINEERING (ICCPPE) 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/1.5140946.
Full textSitorus, Riris, Diah Evawana Anuhgera, Dwi Handayani, Sriwulan, Ika Nur Saputri, and Nikmah Jalilah Ritonga. "Giving Rosella (Hibiscus sabdariffa) Beverage to Overcome Hypertension in Pregnant Women." In International Conference on Health Informatics and Medical Application Technology. SCITEPRESS - Science and Technology Publications, 2019. http://dx.doi.org/10.5220/0009469101800187.
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