Evidence map›Paper›PMID 28608139›Full record

ArticlePharmaceutical research2017

Doxorubicin Hydrochloride Loaded Zymosan-Polyethylenimine Biopolymeric Nanoparticles for Dual 'Chemoimmunotherapeutic' Intervention in Breast Cancer.

Vivek K Pawar, Yuvraj Singh, Komal Sharma, Arpita Shrivastav, Abhisheak Sharma, Akhilesh Singh, Jaya Gopal Meher, Pankaj Singh, Kavit Raval, Himangshu K Bora and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Pharmaceutical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  5. Review
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

13 authors at 2 institutions in 1 country.

Vivek K PawarPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Yuvraj SinghPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Komal SharmaPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Arpita ShrivastavPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Abhisheak SharmaAcademy of Scientific & Innovative Research,, New Delhi, 110025, India.
Akhilesh SinghBiochemistry Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Jaya Gopal MeherPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Pankaj SinghPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Kavit RavalPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Himangshu K BoraLaboratory Animals Facility, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Dipak DattaBiochemistry Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Jawahar LalPharmacokinetics & Metabolism Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India.
Manish K ChourasiaPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, U.P, 226031, India. manish_chourasia@cdri.res.in.
Central Drug Research Institute · INAcademy of Scientific and Innovative Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo utilize nanoparticles produced by condensation of zymosan (an immunotherapeutic polysaccharide) with pegylated polyethylenimine (PEG-PEI) for dual intervention in breast cancer by modulating tumor microenvironment and direct chemotherapy.

methodPositively charged PEG-PEI and negatively charged sulphated zymosan were utilized for electrostatic complexation of chemoimmunotherapeutic nanoparticles (ChiNPs). ChiNPs were loaded with doxorubicin hydrochloride (DOX) for improved delivery at tumor site and were tested for in-vivo tolerability. Biodistribution studies were conducted to showcase their effective accumulation in tumor hypoxic regions where tumor associated macrophages (TAMs) are preferentially recruited.

resultsChiNPs modulated TAMs differentiation resulting in decrement of CD206 positive population. This immunotherapeutic action was furnished by enhanced expression of Th1 specific cytokines. ChiNPs also facilitated an anti-angiogenetic effect which further reduces the possibility of tumor progression and metastasis.

Indexed as

AnimalsAntibiotics, AntineoplasticBreastBreast NeoplasmsCell ProliferationCytokinesDoxorubicinDrug CarriersDrug Delivery SystemsFemaleImmunologic FactorsMacrophagesMice, Inbred BALB CNanoparticlesPolyethyleneimineStatic ElectricityAntibiotics, AntineoplasticCytokinesDoxorubicinDrug CarriersImmunologic FactorsPolyethyleneimineZymosanangiogenesischemoimmunotherapeutic nanoparticlescytokinehypoxiatumor associated macrophages

Identifiers

PMID28608139
OpenAlexW2625817377

What OpenQuestion holds

Textmetadata
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.