SOPs for Nanoparticle Formulation

This SOP outlines the procedure for incorporating bioadhesive polymers into nanoparticle formulations, enhancing their adhesion to biological tissues and improving the residence time of the therapeutic agent at the target site.
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This SOP outlines the procedure for synthesizing dendrimers for drug delivery applications, which are highly branched, nanoscale polymers capable of carrying therapeutic agents through covalent attachment or encapsulation.
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This SOP outlines the procedure for incorporating stabilizers into nanoparticle formulations to enhance the physical and chemical stability of the nanoparticles, preventing aggregation and degradation during storage and application.
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This SOP outlines the procedure for preparing nanoparticles intended for intravenous (IV) administration, focusing on producing nanoparticles with appropriate size, sterility, and biocompatibility for safe administration via the bloodstream.
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This SOP outlines the procedure for incorporating antioxidants into nanoparticle formulations to improve stability, reduce oxidative stress, and enhance the therapeutic effects of nanoparticles used in drug delivery or other biomedical applications.
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This SOP outlines the procedure for synthesizing magnetic nanoparticles for biomedical applications, including targeted drug delivery, hyperthermia therapy, and MRI contrast enhancement.
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This SOP outlines the procedure for developing nanoparticle formulations intended for oral delivery, ensuring that the nanoparticles are stable in the gastrointestinal tract and can deliver the therapeutic agent effectively.
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This SOP outlines the procedure for preparing liposomal nanoparticles, which are lipid-based vesicles used for drug delivery, encapsulating hydrophilic and hydrophobic drugs for targeted therapy.
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This SOP outlines the procedure for incorporating cryoprotectants into nanoparticle formulations to preserve the stability and functionality of nanoparticles during freeze-drying (lyophilization) or cold storage.
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This SOP outlines the procedure for lyophilizing nanoparticle-based formulations, which is used to improve the stability and shelf life of the nanoparticles by removing water through freeze-drying.
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