Publications by authors named "K Faisal"

A rapid, cost-effective, and simple nucleic acid isolation technique coupled with a point-of-need DNA amplification assay is a desirable goal for programmatic use. For diagnosis of Visceral Leishmaniasis (VL), Recombinase Polymerase Amplification (RPA) rapid tests for the detection of Leishmania DNA are versatile and have operational advantages over qPCR. To facilitate the delivery of the RPA test at point-of-need for VL diagnosis, we compared two rapid DNA extraction methods, SwiftDx (SX) and an in-house Boil and Spin (BS) method, coupled with RPA amplification, versus more widely used methods for DNA extraction and amplification, namely Qiagen (Q) kits and qPCR, respectively.

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Background: Glioblastoma is the most common primary malignant brain tumor with characteristic radiological features in most cases.

Case Description: We highlight an unusual case of a 54-year-old woman, neurologically intact, with a diagnostically challenging lesion. The patient's magnetic resonance imaging revealed a left frontal lesion with surrounding edema and a hemosiderin ring, misleading it to be a cavernoma.

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Polymeric micelles are promising carriers for the delivery of poorly water-soluble drugs, providing enhanced drug solubility, blood circulation times, and bioavailability. Nevertheless, the storage and long-term stability of micelles in solution present challenges requiring the lyophilization and storage of formulations in the solid state, with reconstitution immediately prior to application. Therefore, it is important to understand the effects of lyophilization/reconstitution on micelles, particularly their drug-loaded counterparts.

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Article Synopsis
  • The increase in vector habitats and human movement is leading to the introduction of new Leishmania species, which complicates current diagnostic methods for identifying infections.
  • Researchers tested isothermal recombinase polymerase amplification (RPA) assays targeting key Leishmania genetic markers, finding effective detection capabilities for seven pathogenic species.
  • Results showed high sensitivity rates when using these assays on real samples, with a combined sensitivity of 98.57%, suggesting the need for their use in future diagnostics.
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