Evidence map›Paper›PMID 31942659›Full record

ArticlePharmaceutical research2020

Analysis of In Vitro Cytotoxicity of Carbohydrate-Based Materials Used for Dissolvable Microneedle Arrays.

Ezgi P Yalcintas, Daniel S Ackerman, Emrullah Korkmaz, Cheryl A Telmer, Jonathan W Jarvik, Phil G Campbell, Marcel P Bruchez, O Burak Ozdoganlar

Abstract read
PubMed Publisher
In one paragraph

Article in Pharmaceutical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. AnACS applied bio materials · 2025
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

8 authors at 2 institutions in 1 country.

Ezgi P YalcintasDepartment of Mechanical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
Daniel S AckermanDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
Emrullah KorkmazDepartment of Mechanical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
Cheryl A TelmerMolecular Biosensor and Imaging Center, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
Jonathan W JarvikDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
Phil G CampbellMolecular Biosensor and Imaging Center, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
Marcel P BruchezDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
O Burak OzdoganlarDepartment of Mechanical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA. ozdoganlar@cmu.edu.ORCID http://orcid.org/0000-0001-5098-5184
Imaging Center · USCarnegie Mellon University · US

Funding

Defense Sciences Office, DARPA HR0011-16-2-0024
6 · The paper itself

Abstract

purposeDissolvable microneedle arrays (MNAs) can be used to realize enhanced transdermal and intradermal drug delivery. Dissolvable MNAs are fabricated from biocompatible and water-soluble base polymers, and the biocargo to be delivered is integrated with the base polymer when forming the MNAs. The base polymer is selected to provide mechanical strength, desired dissolution characteristics, and compatibility with the biocargo. However, to satisfy regulatory requirements and be utilized in clinical applications, cytotoxicity of the base polymers should also be thoroughly characterized. This study systematically investigated the cytotoxicity of several important carbohydrate-based base polymers used for production of MNAs, including carboxymethyl cellulose (CMC), maltodextrin (MD), trehalose (Treh), glucose (Gluc), and hyaluronic acid (HA).

methodsEach material was evaluated using in vitro cell-culture methods on relevant mouse and human cells, including MPEK-BL6 mouse keratinocytes, NIH-3T3 mouse fibroblasts, HaCaT human keratinocytes, and NHDF human fibroblasts. A common laboratory cell line, human embryonic kidney cells HEK-293, was also used to allow comparisons to various cytotoxicity studies in the literature. Dissolvable MNA materials were evaluated at concentrations ranging from 3 mg/mL to 80 mg/mL.

resultsQualitative and quantitative analyses of cytotoxicity were performed using optical microscopy, confocal fluorescence microscopy, and flow cytometry-based assays for cell morphology, viability, necrosis and apoptosis. Results from different methods consistently demonstrated negligible in vitro cytotoxicity of carboxymethyl cellulose, maltodextrin, trehalose and hyaluronic acid. Glucose was observed to be toxic to cells at concentrations higher than 50 mg/mL.

conclusionsIt is concluded that CMC, MD, Treh, HA, and glucose (at low concentrations) do not pose challenges in terms of cytotoxicity, and thus, are good candidates as MNA materials for creating clinically-relevant and well-tolerated biodissolvable MNAs.

Indexed as

AnimalsApoptosisCarbohydratesCarboxymethylcellulose SodiumCell LineCell ShapeCell SurvivalDrug Delivery SystemsGlucoseHumansHyaluronic AcidMiceMicroinjectionsNeedlesPharmaceutical PreparationsPolymersCarbohydratesCarboxymethylcellulose SodiumGlucoseHyaluronic AcidmaltodextrinPharmaceutical PreparationsPolymersPolysaccharidesTrehalosebiomaterialscarboxymethyl cellulosecytotoxicitydissolvable microneedlesglucosehyaluronic acidin vitromaltodextrinskin cellstrehalose

Identifiers

PMID31942659
OpenAlexW2998858838

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.