Publications by authors named "T M G Mohiuddin"

Article Synopsis
  • Many drugs used in medicine come from bacterial natural products created by complex enzymes called nonribosomal peptide synthetases (NRPSs) that link amino acids together.
  • This research identifies new recombination sites within a specific part of NRPSs, the thiolation (T) domain, paving the way for innovative engineering of these enzymes.
  • The study introduces a method called "eXchange Unit between T domains" (XUT), which enables scientists to combine NRPS fragments with different characteristics to create specific drugs, such as a proteasome inhibitor constructed from five distinct NRPS pieces.
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In this paper we have studied the density functional theory of four drugs ibuprofen, alendronate, Sulfasalazine and paracetamol with quartz, propylamine, trimethylamine functionalized quartz and carboxyl modified carbon nanotube. The attractive and repulsive interaction energies between drugs and quartz is obtained at various pH values. The attractive and repulsive energies are well correlated with experimental drug loading and releasing behavior by mesoporous silica nanoparticles.

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Objective: To determine the healthcare costs and use burden of pediatric feeding disorder after congenital heart surgery.

Study Design: A retrospective, population-based cohort study using claims data (2009-2018) was performed. Participants include patients aged 0-18 years who had undergone congenital heart surgery and were included in the insurance database ≥1 year after surgery.

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Traditional immunohistochemistry (IHC) has already become an essential method of diagnosis and therapy in cancer management. However, this antibody-based technique is limited to detecting a single marker per tissue section. Since immunotherapy has revolutionized the antineoplastic therapy, developing new immunohistochemistry strategies to detect multiple markers simultaneously to better understand tumor environment and predict or assess response to immunotherapy is necessary and urgent.

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Near infrared photoimmunotherapy (NIR-PIT) is a newly developed molecular targeted cancer treatment, which selectively kills cancer cells or immune-regulatory cells and induces therapeutic host immune responses by administrating a cancer targeting moiety conjugated with IRdye700. The local exposure to near-infrared (NIR) light causes a photo-induced ligand release reaction, which causes damage to the target cell, resulting in immunogenic cell death (ICD) with little or no side effect to the surrounding normal cells. Moreover, NIR-PIT can generate an immune response in distant metastases and inhibit further cancer attack by combing cancer cells targeting NIR-PIT and immune regulatory cells targeting NIR-PIT or other cancer treatment modalities.

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