Evidence map›Paper›PMID 40310527›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2025

QbD assisted development of hyaluronic acid and TPGS incorporated DOX liposome(s): in vitro assessment of cytotoxicity, uptake, ROS, and NF-κB potential on MDA-MB-231 cells.

Lakshmi Kumari, Rajveer Singh, Preeti Patel, Amrinder Singh, Dilpreet Singh, Nitin Sharma, Ghanshyam Das Gupta, Balak Das Kurmi

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In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Lakshmi KumariDepartment of Pharmaceutics, ISF College Pharmacy, GT Road, Moga, 142001, Punjab, India.
Rajveer SinghDepartment of Pharmacognosy, ISF College Pharmacy, GT Road, Moga, 142001, Punjab, India.
Preeti PatelDepartment of Pharmaceutical Chemistry, ISF College Pharmacy, GT Road, Moga, 142001, Punjab, India. ppatelpharma@gmail.com.
Amrinder SinghChitkara College of Pharmacy, Chitkara University, Rajpura, 140401, Punjab, India.
Dilpreet SinghSchool of Pharmaceutical Sciences, CT University, Ferozepur Road, Sidhwan Khurd, 142024, Punjab, India.
Nitin SharmaDepartment of Pharmaceutics, Amity Institute of Pharmacy, Amity University, Noida, Uttar Pradesh, India.
Ghanshyam Das GuptaDepartment of Pharmaceutics, ISF College Pharmacy, GT Road, Moga, 142001, Punjab, India.
Balak Das KurmiDepartment of Pharmaceutics, ISF College Pharmacy, GT Road, Moga, 142001, Punjab, India. bdkurmi@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This work aimed to develop Doxorubicin (DOX), D‑alpha‑tocopheryl polyethylene glycol 1000 succinate (TPGS), and hyaluronic acid (HA) liposomal delivery system using the Quality by Design (QbD) methodology. Developed liposomal formulations show sustained release behaviour as compared to free DOX (96.7 ± 1.81% release in 12 h), as indicated by the release kinetics metrics (82.8 ± 2.82% & 69.8 ± 2.25% releases in 72 h of HA-DOX-TPGS-LIPO and DOX-TPGS-LIPO respectively). In vitro cytotoxicity by MTT assay on MDA-MB-231 and MCF-7 breast cancer cells demonstrated that HA-DOX-TPGS-LIPO had significantly higher cytotoxicity and a clear synergistic impact over free drug or DOX-TPGS-LIPO respectively. Higher cell internalization of HA-DOX-TPGS-LIPO was seen in an in vitro cellular uptake assay in contrast to free drug and DOX-TPGS-LIPO investigated by FACS analysis. ROS production was also assessed using 2', 7'-Dichlorofluorescin diacetates (DCFDA) in the FACS study. Upon treatment with HA-DOX-TPGS-LIPO, triple-negative breast cancer (TNBC) cells showed a higher ROS generation than free DOX and DOX-TPGS-LIPO. Moreover, the expression of the NF-κB protein was also analyzed as a possible substitute mechanism for apoptosis. Free DOX treatment resulted in the maximum expression of NF-κB protein, whereas the HA-DOX-TPGS-LIPO formulation showed the minimum expression of NF-κB protein at the same concentration of DOX-TPGS-LIPO. The study suggested that HA-tethered developed liposomal formulation could be an effective tumor treatment and may be a valuable targeted nanocarrier.

Indexed as

Antibiotics, AntineoplasticDoxorubicinHyaluronic AcidNF-kappa BVitamin EBreast NeoplasmsCell Line, TumorCell SurvivalDrug LiberationFemaleHumansLiposomesMCF-7 CellsMDA-MB-231 CellsPolyethylene GlycolsReactive Oxygen SpeciesAntibiotics, AntineoplasticDoxorubicinHyaluronic Acidliposomal doxorubicinLiposomesNF-kappa BPolyethylene GlycolsReactive Oxygen SpeciestocophersolanVitamin ECD44 receptorCellular uptakeCytotoxicity studyDoxorubicinHyaluronic acidLiposomeTNBC

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.