Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
World J Microbiol Biotechnol ; 36(6): 88, 2020 Jun 05.
Article in English | MEDLINE | ID: mdl-32500290

ABSTRACT

This work reports the production of MEL-A using coconut water as the carbon source. Proximate analysis of coconut water indicated the presence of nutrients necessary for growth of the organism and production of desired metabolite. The amount of MEL produced using coconut water was 3.85 g/L (± 0.35) with 74% of it being MEL-A when compared to 2.58 g/L (± 0.15) with 60% being MEL-A using glycerol, a conventional carbon source. MEL-A from coconut water consisted of 38.1% long-chain saturated fatty acids (C16:0 and C18:0) whereas with glycerol it was 9.6%. The critical micellar concentration of the biosurfactant from coconut water was 2.32 ± 0.21 µM when compared to 4.41 ± 0.25 µM from glycerol. The stability of O/W emulsion was reduced by 50% and 90% after incubation for 8 h in the case of MEL-A from coconut water and glycerol respectively when compared to synthetic surfactant, Tween-20. MEL-A from both the sources exhibited free radical scavenging activity (DPPH assay) in a dose-dependent manner wherein MEL-A from coconut water showed two fold higher activity than the other. The interaction of coconut water MEL-A with DPPC for drug encapsulation applications was also studied. The DSC measurements showed the differences in the interaction of drugs with DPPC/MEL-A liposome. The differences were also observed in the solubility of drugs after encapsulation with DPPC/MEL-A liposome.


Subject(s)
Basidiomycota/metabolism , Cocos/metabolism , Glycolipids/biosynthesis , Carbon/analysis , Carbon/chemistry , Cocos/chemistry , Drug Delivery Systems/methods , Emulsions/chemistry , Emulsions/isolation & purification , Fatty Acids/analysis , Fatty Acids/chemistry , Fermentation , Glycerol/metabolism , Glycolipids/chemistry , Glycolipids/isolation & purification , Liposomes , Micelles , Surface-Active Agents/chemistry , Surface-Active Agents/isolation & purification
2.
Expert Opin Ther Pat ; 30(7): 557-565, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32274944

ABSTRACT

INTRODUCTION: Arenavirus are unique category-A pathogens that are also classified as Orphan diseases. Very few options exist currently for treating Viral Hemorrhagic Fever (VHF) caused by viruses belonging to the Arenaviridae family [1]. The current review provides detailed patent landscape and a description of selected technologies developed for combating category-A Arenavirus. Currently, Arenavirus infections are epidemic [2] but could cause widespread pandemics due to ease of dissemination and lack of immunity against these viruses. AREAS COVERED: The key strings for selected Arenavirus VHF were run separately in MCPaIRS®, PatSeer, and Questel database. The search was limited to Title, Abstract and Claim fields; one member per patent family was considered for analysis. EXPERT OPINION: Synthetic molecules dominate the patent landscape, while natural products have not been extensively claimed for the treatment of Arenavirus infection. The broad-spectrum activity has been highly desired for Arenavirus treatment, but few reports have experimentally tested it. With each year, a constant increase in number of patents published is seen, while the maximum number of applications was filed in 2017. The research in VHF is driven by public funds; the maximum numbers of patents were filed by publicly funded organizations.


Subject(s)
Antiviral Agents/pharmacology , Arenaviridae Infections/drug therapy , Hemorrhagic Fevers, Viral/drug therapy , Animals , Arenaviridae Infections/virology , Arenavirus/isolation & purification , Hemorrhagic Fevers, Viral/virology , Humans , Patents as Topic , Rare Diseases/drug therapy , Rare Diseases/virology
SELECTION OF CITATIONS
SEARCH DETAIL
...