Evidence map›Paper›PMID 31632019›Full record

ArticleInternational journal of nanomedicine2019

CD-340 functionalized doxorubicin-loaded nanoparticle induces apoptosis and reduces tumor volume along with drug-related cardiotoxicity in mice.

Laboni Mondal, Biswajit Mukherjee, Kaushik Das, Sanchari Bhattacharya, Debasmita Dutta, Shreyasi Chakraborty, Murari Mohan Pal, Raghuvir H Gaonkar, Mita Chatterjee Debnath

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2019. 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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 47 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Laboni MondalDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.
Biswajit MukherjeeDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.ORCID 0000-0002-7854-9680
Kaushik DasDepartment of Biological Chemistry, Indian Association for the Cultivation of Science, Kolkata 700032, India.
Sanchari BhattacharyaDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.ORCID 0000-0002-8958-0077
Debasmita DuttaDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.
Shreyasi ChakrabortyDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.
Murari Mohan PalDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.
Raghuvir H GaonkarInfectious Diseases and Immunology Division, CSIR-Indian Institute of Chemical Biology, Kolkata 700032, India.
Mita Chatterjee DebnathInfectious Diseases and Immunology Division, CSIR-Indian Institute of Chemical Biology, Kolkata 700032, India.
Jadavpur University · INIndian Institute of Chemical Biology · INIndian Association for the Cultivation of Science · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveTargeted drug delivery of nanoparticles decorated with site-specific recognition ligands is of considerable interest to minimize cytotoxicity of chemotherapeutics in the normal cells. The study was designed to develop CD-340 antibody-conjugated polylactic-co-glycolic acid (PLGA) nanoparticles loaded with a highly water-soluble potent anticancer drug, doxorubicin (DOX), to specifically deliver entrapped DOX to breast cancer cells.

methodsThe study showed how to incorporate water-soluble drug in a hydrophobic PLGA (85:15) based matrix which otherwise shows poor drug loading due to leaching effect. The optimized formulation was covalently conjugated to anti-human epidermal growth factor receptor-2 (HER2) antibody (CD-340). Surface conjugation of the ligand was assessed by flow cytometry, confocal microscopy, and gel electrophoresis. Selectivity and cytotoxicity of the experimental nanoparticles were tested on human breast cancer cells SKBR-3, MCF-7, and MDA-MB-231. Both CD-340-conjugated and unconjugated nanoparticles were undergone in vitro and in vivo characterization.

resultHigher level of incorporation of DOX (8.5% W/W), which otherwise shows poor drug loading due to leaching effect of the highly water-soluble drug, was seen in this method. In HER2-overexpressing tumor xenograft model, radiolabeled antibody-conjugated nanoparticles showed preferentially more of the formulation accumulation in the tumor area when compared to the treatments with the unconjugated one or with the other control groups of mice. The ligand conjugated nanoparticles showed considerable potential in reduction of tumor growth and cardiac toxicity of DOX in mice, a prominent side-effect of the drug.

conclusionIn conclusion, CD-340-conjugated PLGA nanoparticles containing DOX preferentially delivered encapsulated drug to the breast cancer cells and in breast tumor and reduced the breast tumor cells by apoptosis. Site-specific delivery of the formulation to neoplastic cells did not affect normal cells and showed a drastic reduction of DOX-related cardiotoxicity.

Indexed as

AnimalsAntibodiesAntineoplastic AgentsApoptosisBreast NeoplasmsCardiotoxicityCell DeathCell Line, TumorDoxorubicinDrug LiberationEndocytosisErb-b2 Receptor Tyrosine KinasesFemaleHumansKineticsMice, Inbred BALB CAntibodiesAntineoplastic AgentsDoxorubicinErb-b2 Receptor Tyrosine KinasesPolylactic Acid-Polyglycolic Acid Copolymerbreast cancerligandnanoparticlestargetingtumor

Identifiers

PMID31632019
PMCPMC6790403
OpenAlexW2979587490

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.