Tag: Nanoparticle quality control SOP

SOP for Use of Surfactants in Nanoparticle Formulations Standard Operating Procedure for Use of Surfactants in Nanoparticle Formulations 1) Purpose This SOP outlines the procedure for incorporating surfactants in nanoparticle formulations. Surfactants are essential for stabilizing nanoparticles by reducing surface tension, preventing aggregation, and ensuring uniform particle size distribution. 2) Scope This SOP applies to…

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SOP for Formation of Solid Lipid Nanoparticles (SLNs) Standard Operating Procedure for Formation of Solid Lipid Nanoparticles (SLNs) 1) Purpose The purpose of this SOP is to outline the procedure for the preparation of solid lipid nanoparticles (SLNs). SLNs are colloidal carriers made from solid lipids, offering controlled drug release and enhanced bioavailability for various…

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SOP for Preparation of Nanoparticles for Targeted Drug Delivery Standard Operating Procedure for Preparation of Nanoparticles for Targeted Drug Delivery 1) Purpose This SOP outlines the steps for preparing nanoparticles designed for targeted drug delivery, which can enhance therapeutic efficacy and minimize off-target effects of drugs. 2) Scope This SOP applies to all personnel involved…

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SOP for Use of Bioadhesive Polymers in Nanoparticle Formulations Standard Operating Procedure for Use of Bioadhesive Polymers in Nanoparticle Formulations 1) Purpose The purpose of this SOP is to outline the procedure for incorporating bioadhesive polymers in nanoparticle formulations. Bioadhesive polymers enhance the mucoadhesion of nanoparticles, allowing for prolonged retention time at the site of…

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SOP for Preparation of Dendrimers for Drug Delivery Standard Operating Procedure for Preparation of Dendrimers for Drug Delivery 1) Purpose This SOP outlines the procedure for preparing dendrimers, which are branched polymers used for drug delivery applications. Dendrimers provide controlled drug release and targeted delivery properties. 2) Scope This SOP applies to laboratory personnel responsible…

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SOP for Incorporation of Stabilizers in Nanoparticle-Based Formulations Standard Operating Procedure for Incorporation of Stabilizers in Nanoparticle-Based Formulations 1) Purpose This SOP outlines the procedure for incorporating stabilizers into nanoparticle-based formulations to enhance their stability, prevent aggregation, and improve shelf life. 2) Scope This SOP applies to laboratory personnel responsible for preparing nanoparticle formulations that…

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SOP for Preparation of Nanoparticles for Intravenous Administration Standard Operating Procedure for Preparation of Nanoparticles for Intravenous Administration 1) Purpose This SOP outlines the procedure for preparing sterile nanoparticles for intravenous (IV) administration, ensuring the formulation is suitable for direct injection into the bloodstream for therapeutic use. 2) Scope This SOP applies to laboratory personnel…

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SOP for Use of Antioxidants in Nanoparticle Formulations Standard Operating Procedure for Use of Antioxidants in Nanoparticle Formulations 1) Purpose The purpose of this SOP is to outline the procedure for incorporating antioxidants in nanoparticle formulations. Antioxidants are used to prevent oxidative degradation of both the active pharmaceutical ingredients (API) and the carrier material, ensuring…

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SOP for Preparation of Magnetic Nanoparticles for Biomedical Applications Standard Operating Procedure for Preparation of Magnetic Nanoparticles for Biomedical Applications 1) Purpose This SOP outlines the procedure for the preparation of magnetic nanoparticles used in biomedical applications, such as targeted drug delivery, magnetic resonance imaging (MRI), and hyperthermia treatment. 2) Scope This SOP applies to…

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SOP for Development of Nanoparticle Formulations for Oral Delivery Standard Operating Procedure for Development of Nanoparticle Formulations for Oral Delivery 1) Purpose The purpose of this SOP is to outline the procedure for developing nanoparticle-based formulations for oral drug delivery. Nanoparticles offer improved bioavailability, protection of the active pharmaceutical ingredient (API) from the harsh gastrointestinal…

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