Evidence map›Paper›PMID 29997433›Full record

ArticleDrug design, development and therapy2018

Gemcitabine hydrochloride microspheres used for intravesical treatment of superficial bladder cancer: a comprehensive in vitro/ex vivo/in vivo evaluation.

Sinem Yaprak Karavana, Zeynep Ay Şenyiğit, Çağrı Çalışkan, Gülnur Sevin, Derya İlem Özdemir, Yalçın Erzurumlu, Sait Şen, Esra Baloğlu

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 31 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Sinem Yaprak KaravanaDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Ege University, Izmir, Turkey, sinemyaprak@hotmail.com.
Zeynep Ay ŞenyiğitDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Izmir Katip Çelebi University, Izmir, Turkey.
Çağrı ÇalışkanDepartment of Radiopharmacy, Faculty of Pharmacy, Ege University, Izmir, Turkey.
Gülnur SevinDepartment of Pharmacology, Faculty of Pharmacy, Ege University, Izmir, Turkey.
Derya İlem ÖzdemirDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Izmir Katip Çelebi University, Izmir, Turkey.
Yalçın ErzurumluDepartment of Biochemistry, Faculty of Pharmacy, Ege University, Izmir, Turkey.
Sait ŞenDepartment of Pathology, Faculty of Medicine, Ege University, Izmir, Turkey.
Esra BaloğluDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Ege University, Izmir, Turkey, sinemyaprak@hotmail.com.
Ege University · TRIzmir Kâtip Çelebi University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBladder cancer is responsible for more than 130,000 deaths annually worldwide. Intravesical delivery of chemotherapeutic agents provides effective drug localization to the target area to reduce toxicity and increase efficacy. This study aimed to develop an intravesical delivery system of gemcitabine HCl (Gem-HCl) to provide a sustained-release profile, to prolong residence time, and to enhance its efficiency in the treatment of bladder cancer. MATERIALS AND

methodsFor this purpose, bioadhesive microspheres were successfully prepared with average particle size, encapsulation efficiency, and loading capacity of 98.4 µm, 82.657%±5.817%, and 12.501±0.881 mg, respectively. For intravesical administration, bioadhesive microspheres were dispersed in mucoadhesive chitosan or in situ poloxamer gels and characterized in terms of gelation temperature, viscosity, mechanical, syringeability, and bioadhesive and rheological properties. The cytotoxic effects of Gem-HCl solution, Gem-HCl microspheres, and Gem-HCl microsphere-loaded gel formulations were evaluated in two different bladder cancer cell lines: T24 (ATCC HTB4TM) and RT4 (ATCC HTB2TM).

resultsAccording to cell-culture studies, Gem-HCl microsphere-loaded poloxamer gel was more cytotoxic than Gem-HCl microsphere-loaded chitosan gel. Antitumor efficacy of newly developed formulations were investigated by in vivo studies using bladder-tumor-induced rats.

conclusionAccording to in vivo studies, Gem-HCl microsphere-loaded poloxamer gel was found to be an effective and promising alternative for current intravesical delivery-system therapies.

Indexed as

MicrospheresAdministration, IntravesicalAnimalsAntimetabolites, AntineoplasticCell Line, TumorDeoxycytidineDrug CompoundingGemcitabineHumansIn Vitro TechniquesMicroscopy, Electron, ScanningNeoplasms, ExperimentalParticle SizeRatsRats, Sprague-DawleyRheologyAntimetabolites, AntineoplasticDeoxycytidineGemcitabinegemcitabine HClin situ gelintravesical chemotherapymucoadhesive gelsuperficial bladder cancer micro-spheres

Identifiers

PMID29997433
PMCPMC6033088
OpenAlexW2810298246

What OpenQuestion holds

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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.