Evidence map›Paper›PMID 26597940›Full record

ArticlePharmaceutical research2016

Curcumin Delivery by Poly(Lactide)-Based Co-Polymeric Micelles: An In Vitro Anticancer Study.

Preeti Kumari, Muddineti Omkara Swami, Sravan Kumar Nadipalli, Srividya Myneni, Balaram Ghosh, Swati Biswas

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In one paragraph

Article in Pharmaceutical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 72 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Preeti KumariDepartment of Pharmacy, BITS-Pilani, Hyderabad Campus, Shameerpet, Hyderabad, 500078, Telangana, India.
Muddineti Omkara SwamiDepartment of Pharmacy, BITS-Pilani, Hyderabad Campus, Shameerpet, Hyderabad, 500078, Telangana, India.
Sravan Kumar NadipalliDepartment of Pharmacy, BITS-Pilani, Hyderabad Campus, Shameerpet, Hyderabad, 500078, Telangana, India.
Srividya MyneniDepartment of Pharmacy, BITS-Pilani, Hyderabad Campus, Shameerpet, Hyderabad, 500078, Telangana, India.
Balaram GhoshDepartment of Pharmacy, BITS-Pilani, Hyderabad Campus, Shameerpet, Hyderabad, 500078, Telangana, India.
Swati BiswasDepartment of Pharmacy, BITS-Pilani, Hyderabad Campus, Shameerpet, Hyderabad, 500078, Telangana, India. swati.biswas@hyderabad.bits-pilani.ac.in.
Birla Institute of Technology and Science - Hyderabad Campus · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis work describes the synthesis of block co-polymeric micelles, methoxy-poly(ethylene glycol)-poly(D,L-lactide) (mPEG-PLA) to encapsulate Curcumin (CUR), thereby improving the dispersibility and chemical stability of curcumin, prolonging its cellular uptake and enhancing its bioavailability.

methodsCUR-mPEG-PLA micelles, was prepared using the thin-film hydration method and evaluated in vitro. The preparation process was optimized with a central composite design (CCD). Micelles were characterized by size, transmission electron microscopy, loading capacity, and critical micelle concentration (CMC). The cytotoxicity of CUR-mPEG-PLA micelles was investigated against murine melanoma cells, B16F10 and human breast cancer cells, MDA-MB-231.

resultsThe average size of the CUR-mPEG-PLA micelles was 110 ± 5 nm with polydispersity index in the range of 0.15-0.31, and the encapsulating efficiency for CUR was 91.89 ± 1.2, and 11.06 ± 0.8% for drug-loading. Sustained release of CUR from micelles was observed with 9.73% CUR release from micelles compared to 64.24% release of free curcumin in first 6 h under sink condition. The CUR-mPEG-PLA was efficiently taken up by the cancer cells, B16F10 and MDA-MB-231. Following 24 h incubation, CUR-mPEG-PLA induced higher cytotoxicity compared to free CUR in MDA-MB-231 cell lines indicating exposure of higher dose of free CUR to cells lead to up-regulation of drug efflux mechanisms leading to decreased cell death in case of free CUR administration.

conclusionOur results indicate that the proposed micellar system has the potential to serve as an efficient carrier for CUR by effectively solubilizing, stabilizing and delivering the drug in a controlled manner to the cancer cells.

Indexed as

AnimalsAntineoplastic AgentsBreastBreast NeoplasmsCell DeathCell Line, TumorCurcuminDrug CarriersFemaleHumansMelanomaMiceMicellesPolyestersPolyethylene GlycolsAntineoplastic AgentsCurcuminDrug Carriersmethoxy poly(ethylene glycol)-poly(lactide)MicellesPolyestersPolyethylene GlycolscancercurcuminmPEG-PLApolymeric micelles

Identifiers

PMID26597940
OpenAlexW2474814867

What OpenQuestion holds

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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.