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Updated: May 5, 2026

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Using Multiple Light Scattering to Examine the Stability of Phyllanthus emblica L. Extracts Obtained with Different Extraction Methods
Published on: April 14, 2023
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Development of Phyllanthus emblica Extract-Loaded Niosomes for Cancer Treatment: Formulation and In Vitro Evaluation
Al-Zahraa Khalifa1, Naglaa Gamil Shehab1,2, Dema Layth Jabbar3
1Pharmaceutical Sciences Department, College of Pharmacy, Dubai Medical University, Dubai 20170, United Arab Emirates.
Pharmaceuticals (Basel, Switzerland)
|May 4, 2026
Summary
This study developed amla extract-loaded niosomes to improve anticancer drug delivery. The niosomes showed enhanced in vitro anticancer activity against cancer cells, supported by computational analyses.
Area of Science:
- Pharmacology
- Nanotechnology
- Biochemistry
Background:
- Phyllanthus emblica (amla) possesses anticancer properties but faces challenges with stability and bioavailability.
- Niosomes offer a potential solution for encapsulating and delivering bioactive compounds effectively.
Purpose of the Study:
- To develop amla extract-loaded niosomes for enhanced anticancer delivery.
- To evaluate the in vitro anticancer efficacy of these niosomes against MCF-7 and HCT116 cell lines.
- To support findings with in silico molecular docking and pharmacokinetic analyses.
Main Methods:
- Amla extract preparation and lyophilization.
- Niosome formulation via thin-film hydration and physicochemical characterization.
- In vitro cytotoxicity assays and in silico analyses (molecular docking, pharmacokinetic predictions).
Main Results:
- Optimized niosomes demonstrated favorable characteristics, including high entrapment efficiency and sustained release.
- Amla-loaded niosomes exhibited significant concentration-dependent in vitro anticancer activity against both cell lines.
- In silico studies supported the anticancer potential of amla phytochemicals and the rationale for encapsulation.
Conclusions:
- Amla extract-loaded niosomes are a promising system for enhanced and sustained delivery of anticancer agents.
- In silico findings provide mechanistic plausibility and translational rationale for this approach.
- Further in vivo studies are recommended to validate the efficacy of these niosomal formulations.

