Evidence map›Paper›PMID 36171346›Full record

ArticlePharmaceutical research2022

Design, Fabrication and Evaluation of Stabilized Polymeric mixed micelles for Effective Management in Cancer Therapy.

Padakanti Sandeep Chary, Naveen Rajana, Geetanjali Devabattula, Valamla Bhavana, Hoshiyar Singh, Chandraiah Godugu, Santosh Kumar Guru, Shashi Bala Singh, Neelesh Kumar Mehra

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Article in Pharmaceutical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
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

7 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Next-generation cancer nanotherapeutics: PluronicNaunyn-Schmiedeberg's archives of pharmacology · 2025
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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

9 authors at 2 institutions in 1 country.

Padakanti Sandeep CharyPharmaceutical Nanotechnology Research Laboratory, Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India, 500 037.
Naveen RajanaPharmaceutical Nanotechnology Research Laboratory, Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India, 500 037.
Geetanjali DevabattulaDepartment of Biological Sciences, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Valamla BhavanaPharmaceutical Nanotechnology Research Laboratory, Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India, 500 037.
Hoshiyar SinghDepartment of Biological Sciences, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Chandraiah GoduguDepartment of Biological Sciences, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Santosh Kumar GuruDepartment of Biological Sciences, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Shashi Bala SinghDepartment of Biological Sciences, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Neelesh Kumar MehraPharmaceutical Nanotechnology Research Laboratory, Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India, 500 037. neelesh@niperhyd.ac.in.ORCID http://orcid.org/0000-0001-5275-8065
National Institute of Pharmaceutical Education and Research · INNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCancer is one of the most common and fatal disease, chemotherapy is the major treatment against many cancer types. The anti-apoptotic BCL-2 protein's expression was increased in many cancer types and Venetoclax (VLX; BCL-2 inhibitor) is a small molecule, which selectively inhibits this specified protein. In order to increase the clinical performance of this promising inhibitor as a repurposed drug, polymeric mixed micelles formulations approach was explored.

methodsThe Venetoclax loaded polymeric mixed micelles (VPMM) were prepared by using Pluronic® F-127 and alpha tocopherol polyethylene glycol 1000 succinate (TPGS) as excipients by thin film hydration method and characteristics. The percentage drug loading capacity, entrapment efficiency and in-vitro drug release studies were performed using HPLC method. The cytotoxicity assay, cell uptake and anticancer activities were evaluated in two different cancer cells i.e. MCF-7 (breast cancer) and A-549 (lung cancer).

resultsParticle size, polydispersity index and zeta potential of the VPMM was found to be 72.88 ± 0.09 nm, 0.078 ± 0.009 and -4.29 ± 0.24 mV, respectively. The entrapment efficiency and %drug loading were found to be 80.12 ± 0.23% and 2.13% ± 0.14%, respectively. The IC

conclusionThe current investigation revealed that the Venetoclax loaded polymeric mixed micelles (VPMM) revealed the enhanced therapeutic efficacy against breast and lung cancer in vitro models.

Indexed as

Lung NeoplasmsMicellesBridged Bicyclo Compounds, HeterocyclicCell Line, TumorDrug CarriersHumansParticle SizePolyethylene GlycolsPolymersProto-Oncogene Proteins c-bcl-2SulfonamidesVitamin EBridged Bicyclo Compounds, HeterocyclicDrug CarriersMicellesPolyethylene GlycolsPolymersProto-Oncogene Proteins c-bcl-2SulfonamidesvenetoclaxVitamin Epluronic® F-127polymeric mixed micellesthin film hydration methodTPGSvenetoclax

Identifiers

PMID36171346
OpenAlexW4297512872

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Registered trials

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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.