Skip to content
  • Clinical Studies
  • Schedule M
  • Stability Studies
  • Pharma GMP
  • Pharma Tips
  • Pharma Books
  • Pharma Validation
  • Pharma Regulatory

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Preparation and Handling of Nanoparticle Precursors

Posted on By

SOP for Preparation and Handling of Nanoparticle Precursors

Standard Operating Procedure for Handling Nanoparticle Precursors

1) Purpose

This SOP outlines the procedures for the preparation and safe handling of nanoparticle precursors used in the production of nanoparticle formulations. The objective is to ensure proper preparation, safe handling, and prevention of contamination.

2) Scope

This SOP applies to all laboratory staff and operators who are responsible for the preparation and handling of nanoparticle precursors within the laboratory and production areas.

3) Responsibilities

  • Operators: Responsible for handling and preparing nanoparticle precursors in compliance with this SOP.
  • QA: Ensures quality of the prepared precursors and compliance with safety guidelines.
See also  SOP for Preparation of Nanoemulsions

4) Procedure

4.1 Preparation of Nanoparticle Precursors

4.1.1 Required Materials

  • 4.1.1.1 Gather all required precursor materials, such as polymers, surfactants, lipids, or metals, depending on the nanoparticle type.
  • 4.1.1.2 Ensure all equipment and containers are cleaned and sanitized according to laboratory guidelines.

4.1.2 Weighing and Dispensing

  • 4.1.2.1 Use a calibrated balance to weigh the exact amounts of precursors as per the formulation batch record.
  • 4.1.2.2 Dispense the required materials into properly labeled containers for each batch.

4.2 Handling of Precursors

4.2.1 Safety Measures

  • 4.2.1.1 Ensure all operators are wearing appropriate personal protective equipment (PPE), including gloves, safety goggles, and lab coats.
  • 4.2.1.2 Work in a fume hood or well-ventilated area when handling volatile or
hazardous chemicals.

4.2.2 Contamination Prevention

  • 4.2.2.1 Use sterile, sealed containers to transport precursors to the production area to prevent cross-contamination.
  • 4.2.2.2 Handle precursors only with sterilized tools to avoid contamination.

4.3 Storage of Nanoparticle Precursors

4.3.1 Storage Conditions

  • 4.3.1.1 Store all nanoparticle precursors at the appropriate temperature (as indicated in the precursor’s material safety data sheet) to maintain stability and prevent degradation.
  • 4.3.1.2 Ensure all containers are labeled with material name, batch number, and date of preparation.

5) Abbreviations, if any

  • PPE: Personal Protective Equipment
  • QA: Quality Assurance

6) Documents, if any

  • Nanoparticle Precursor Preparation Logbook

7) References, if any

  • Material Safety Data Sheets (MSDS) for nanoparticle precursors

8) SOP Version

Version 1.0

Annexure

Nanoparticle Precursor Preparation Logbook Template

Date Material Name Batch Number Quantity Prepared Operator Initials QA Initials
DD/MM/YYYY Precursor Material Batch Number Quantity in grams Operator Name QA Name
           
See also  SOP for Spill Management and Containment of Nanoparticles
Nanoparticle Formulation Tags:Nanoparticle biomedical applications SOP, Nanoparticle clinical trial SOP, Nanoparticle encapsulation SOP, Nanoparticle formulation SOP, Nanoparticle handling SOP, Nanoparticle preparation procedure, Nanoparticle production SOP, Nanoparticle quality control SOP, Nanoparticle size optimization SOP, Nanoparticle SOP, Nanoparticle stability testing SOP, Nanoparticle standard operating procedures, Nanoparticle sterilization SOP, Nanoparticle storage SOP, Nanoparticle surface modification SOP, Nanoparticle synthesis SOP, Nanoparticle toxicology SOP, SOP for nanomaterials, SOP for nanoparticle characterization, SOP for nanoparticle drug delivery, SOP for nanoparticle gene delivery, SOP for nanoparticle regulatory compliance, SOP for nanoparticle safety, SOP for nanoparticle scaling, SOP for targeted drug delivery nanoparticles

Post navigation

Previous Post: SOP for Raw Material Receipt, Identification, and Storage for Nanoparticle-Based Formulations
Next Post: SOP for Incorporation of Taste-Masking Agents in Nasal Sprays

Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme

Go to mobile version