Evidence map›Paper›PMID 41366168›Full record

ArticleAAPS PharmSciTech2025

Sustained-release Drug Delivery System of Trazodone Hydrochloride Based on Electrospray Technology: Preparation, Characterization, In vitro and In vivo Evaluation.

Chengwei Wang, Haiqiao Wang, Michael Adu-Frimpong, Zhihui Zou, Zhou Jin, Peiqi Lu, Zhenrong Liu, Haojie Tian, Ying Xu, Kailun Yang and 3 more

Abstract read
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Article in AAPS PharmSciTech, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Chengwei WangDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0009-0007-6243-6378
Haiqiao WangDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0009-0000-3345-6002
Michael Adu-FrimpongDepartment of Biochemistry and Forensic Sciences, School of Chemical and Biochemical Sciences, C. K. Tedam University of Technology and Applied Sciences (CKT-UTAS), 0215-5321, Navrongo, Ghana.ORCID http://orcid.org/0000-0002-6635-4261
Zhihui ZouDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0009-0007-9807-3855
Zhou JinDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0009-0001-5686-8875
Peiqi LuDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0009-0004-8092-7662
Zhenrong LiuDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0009-0006-0967-6885
Haojie TianDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0009-0006-5714-3768
Ying XuDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0000-0002-2036-5950
Kailun YangNational Center for Biotechnology Development, Beijing, 100039, China.ORCID http://orcid.org/0009-0003-3630-8197
Jiangnan YuDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0000-0001-6050-6458
Ximing XuDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China.ORCID http://orcid.org/0000-0002-7113-6226
Yuan ZhuDepartment of Pharmaceutics, School of Pharmacy, Jiangsu University, Jiangsu, 212013, China. zhuyuanemail@126.com.ORCID http://orcid.org/0000-0003-4309-3967

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Electrospray technology is a process capable of forming monodisperse drug nano/microparticles with enhanced solubility or sustained-release effects. This study aimed to fabricate a sustained-release drug delivery system containing trazodone hydrochloride (TZN-SRDDS) by combining electrospray technology with functional carriers (Soluplus®, Carbopol 940, HPMC K4M, and Lecithin) for solubility improving, drug release prolonging and bioavailability enhancing. The optimized TZN-SRDDS exhibited a spherical morphology, with a particle size of (3.456 ± 0.448) μm, a polydispersity index (PDI) of (0.456 ± 0.024), and a zeta potential of (-17.291 ± 2.351) mV. This system showed a high encapsulation efficiency (97.12 ± 1.82%) and maintained good stability for up to 30 days. In vitro release studies indicated that TZN-SRDDS followed first-order kinetics in pH 1.2 hydrochloric acid solution and the Higuchi model in pH 6.8 phosphate-buffered saline (PBS), with the cumulative release rate increased to (80.81 ± 4.26%); both release profiles exhibited a certain sustained-release effect. Cytotoxicity assays confirmed that TZN-SRDDS was non-toxic at concentrations below 2.6 mg/mL, and the formulation showed a relatively sustained cellular uptake effect. Pharmacokinetic studies in rats showed that the time to reach peak concentration (T

Indexed as

Delayed-Action PreparationsDrug Delivery SystemsTrazodoneAnimalsBiological AvailabilityChemistry, PharmaceuticalDrug CarriersDrug LiberationLecithinsMaleParticle SizeRatsRats, Sprague-DawleySolubilityDelayed-Action PreparationsDrug CarriersLecithinsTrazodoneelectrospray technologysustained-release drug delivery systemtissue distributiontrazodone hydrochloride

Identifiers

PMID41366168

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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.