Evidence map›Paper›PMID 30961297›Full record

ArticlePolymers2018

Photocurable Bioinks for the 3D Pharming of Combination Therapies.

Giovanny F Acosta-Vélez, Chase S Linsley, Timothy Z Zhu, Willie Wu, Benjamin M Wu

Open access · goldAbstract read
In one paragraph

Article in Polymers, 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
0.9field-weighted citation impact, top 27% 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, 27 citations in OpenAlex.

  1. Review
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  4. 3D-printed dosage forms for oral administration: a review.Drug delivery and translational research · 2024
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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

5 authors at 1 institution in 1 country.

Giovanny F Acosta-VélezDepartment of Bioengineering, University of California, Los Angeles, 420 Westwood Plaza, Room 5121, Engineering V, 951600 Los Angeles, CA 90095, USA. gacosta3@g.ucla.edu.ORCID 0000-0002-7836-7617
Chase S LinsleyDepartment of Bioengineering, University of California, Los Angeles, 420 Westwood Plaza, Room 5121, Engineering V, 951600 Los Angeles, CA 90095, USA. clinsle@g.ucla.edu.ORCID 0000-0002-8259-5487
Timothy Z ZhuDepartment of Bioengineering, University of California, Los Angeles, 420 Westwood Plaza, Room 5121, Engineering V, 951600 Los Angeles, CA 90095, USA. timmy90109@gmail.com.
Willie WuDepartment of Bioengineering, University of California, Los Angeles, 420 Westwood Plaza, Room 5121, Engineering V, 951600 Los Angeles, CA 90095, USA. williewu@ucla.edu.
Benjamin M WuDepartment of Bioengineering, University of California, Los Angeles, 420 Westwood Plaza, Room 5121, Engineering V, 951600 Los Angeles, CA 90095, USA. benwu@g.ucla.edu.
University of California, Los Angeles · US

Funding

GlaxoSmithKline PO No. 36257529 OS
6 · The paper itself

Abstract

Combination therapies mediate drug synergy to improve treatment efficacy and convenience, leading to higher levels of compliance. However, there are challenges with their manufacturing as well as reduced flexibility in dosing options. This study reports on the design and characterization of a polypill fabricated through the combination of material jetting and binder jetting for the treatment of hypertension. The drugs lisinopril and spironolactone were loaded into hydrophilic hyaluronic acid and hydrophobic poly(ethylene glycol) (PEG) photocurable bioinks, respectively, and dispensed through a piezoelectric nozzle onto a blank preform tablet composed of two attachable compartments fabricated via binder jetting 3D printing. The bioinks were photopolymerized and their mechanical properties were assessed via Instron testing. Scanning electron microscopy (SEM) was performed to indicate morphological analysis. The polypill was ensembled and drug release analysis was performed. Droplet formation of bioinks loaded with hydrophilic and hydrophobic active pharmaceutical ingredients (APIs) was achieved and subsequently polymerized after a controlled dosage was dispensed onto preform tablet compartments. High-performance liquid chromatography (HPLC) analysis showed sustained release profiles for each of the loaded compounds. This study confirms the potential of material jetting in conjunction with binder jetting techniques (powder-bed 3D printing), for the production of combination therapy oral dosage forms involving both hydrophilic and hydrophobic drugs.

Indexed as

3D printinghyaluronic acidinkjet printingpharmaceutical tabletsphotopolymerizationpoly(ethylene glycol)

Identifiers

PMID30961297
PMCPMC6401852
OpenAlexW2904366103

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.