4 research outputs found

    Hypothesis Volume 8(2) Identification of miRNAs in C. roseus and their potential targets

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    Abstract: MicroRNAs are small (20-22 nucleotides) none coding, regulatory RNAs, whose pivotal role in gene expression has been associated in number of diseases, therefore prediction of miRNA is an essential yet challenging field. In this study miRNAs of C. roseus are predicted along with their possible target genes. A total of 19,899 ESTs were downloaded from dbEST database and processed and trimmed through SeqClean. Nine sequences were trashed and 31 sequences were trimmed by the program and the resulting sequences were submitted to Repeatmasker and TGICL for clustering and assembly. This contig database was now used to find the putative miRNAs by performing a local BLAST with the miRNAs of B. rapa retrieved from miRBase. The targets were scanned by hybridizing screened ESTs with the UTRs of human using miRanda software. Finally, 7 putative miRNAs were found to hybridize with the various targets of signal transduction and apoptosis that may play significant role in preventing diseases like Leukemia, Arthritis and Alzheimer. Background: MicroRNA

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    Not AvailableThe present study is focused on functionalisation of mesoporous silica (or SBA-15) to control azathioprine drug release rate and its toxic effect. The mesoporous silica was functionalised by (γ-chloropropyl)triethoxysilicane and (3-aminopropyl)triethoxysilane (APTES) via hydrothermal process. The azathioprine was loaded into SBA-15 via post impregnation method. Azathioprine-loaded pristine and functionalised SBA-15 samples were characterised using UV–visible spectrophotometry and thermogravimetric analysis to measure the drug loading efficiency. The samples were also characterised by small and wide-angle powder X-ray diffraction, scanning electron microscope, transmission electron microscope, infrared spectroscopy and nitrogen adsorption/desorption analysis to study the structure, morphology, functionalisation and drug loading in detail. The maximum drug loading efficiency of 65(±1)% was achieved. In vitro azathioprine release profiles were studied in phosphate buffered saline (pH 7.4) and results suggested that the drug release amount could be controlled by functionalisation of carrier matrix SBA-15. Azathioprine-loaded APTES-functionalised material revealed lowest release amount of ~64.5% in 60 h. The toxicity of azathioprine was significantly reduced by loading the drug into the mesoporous pristine and functionalised silica. The controlled azathioprine release reduced its repeated administration and can reduce its toxicity and side effects. These outcomes recommend that the functionalised SBA-15 is an advantageous drug carrier for achieving extended release time.Not Availabl
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