Evidence map›Paper›PMID 42733877›Full record

ArticleInternational journal of nanomedicine2026

Hyaluronic Acid-Modified Celecoxib-Loaded Nanostructured Lipid Carriers Combined with Dissolving Microneedles for Targeted Sustained-Release Therapy in Osteoarthritis.

Junfeng Ban, Yichao Li, Yanhua Guo, Huashen He, Chuangzan Yang, Peining Li, Jiawei Liang, Shirui Li, Xueyuan Luo, Yu Li and 3 more

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Junfeng BanSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0000-0001-7334-9375
Yichao Li *School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0009-0000-5475-4906
Yanhua Guo *Department of New Materials and Passive Medical Device Inspection and Research, Guangzhou Institute of Quality Inspection, Guangzhou, People's Republic of China.
Huashen HeSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0009-0007-9647-6482
Chuangzan YangSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0009-0000-9002-1398
Peining LiDepartment of New Materials and Passive Medical Device Inspection and Research, Guangzhou Institute of Quality Inspection, Guangzhou, People's Republic of China.ORCID 0000-0003-1925-1048
Jiawei LiangSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Shirui LiSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0009-0003-5157-7109
Xueyuan LuoSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0009-0009-2059-8410
Yu LiSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0009-0004-8539-9838
Yi XieSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Xiangmei LiuDepartment of New Materials and Passive Medical Device Inspection and Research, Guangzhou Institute of Quality Inspection, Guangzhou, People's Republic of China.ORCID 0000-0001-9153-3264
Xiaofang LiSchool of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0009-0001-1219-5429

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Rapid local drug clearance and poor sustained retention pose challenges to the treatment of osteoarthritis. Therefore, a local delivery system that prolongs intra-articular drug retention and achieves efficient targeted delivery holds significant clinical promise. Methods: Hyaluronic acid-modified celecoxib nanostructured lipid carriers (HA-Cxb-NLCs) were prepared and encapsulated in dissolving microneedles to form a composite delivery system (HA-Cxb-NLCs-DMNs). The system was characterised in terms of its physicochemical properties, in vitro drug release profiles, transdermal permeation behaviour, cellular compatibility, and uptake mechanisms. Subsequently, a sodium iodoacetate-induced rat osteoarthritis model was used to evaluate the therapeutic efficacy in vivo. Results: HA-Cxb-NLCs-DMNs exhibit a uniform particle size (113.93 ± 1.66 nm) and a zeta potential of (-39.16 ± 3.00 mV). In vitro release persisted for 72 hours, with a cumulative permeation of 62.74 ± 1.40 μg·cm Conclusion: This study presents a promising microneedle-nanoparticle synergistic delivery strategy for the local targeted therapy of osteoarthritis.

Indexed as

CelecoxibDrug CarriersHyaluronic AcidNanostructuresOsteoarthritisAdministration, CutaneousAnimalsDelayed-Action PreparationsLipidsMaleMicroneedle Drug DeliveryParticle SizeRatsRats, Sprague-DawleySkin AbsorptionCelecoxibDelayed-Action PreparationsDrug CarriersHyaluronic AcidLipidsdissolving microneedleshyaluronic acid-modified celecoxib nanolipid carrierosteoarthritistransdermal administration

Identifiers

PMID42733877
PMCPMC13571682

What Socratic holds

Textmetadata
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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 Socratic graph.