Evidence map›Paper›PMID 41960159›Full record

ReviewMaterials today. Bio2026

From permeation enhancer to therapeutic enabler: Advances, applications, and translational perspectives in hyaluronidase-based drug delivery.

Yuna Seo, Jiyoon Sung, Jae-Young Lee

Abstract readReview
In one paragraph

Review in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Yuna SeoCollege of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea.
Jiyoon SungCollege of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea.
Jae-Young LeeCollege of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyaluronidase is a carbohydrate-active enzyme that cleaves glycosaminoglycans, particularly hyaluronic acid. By transiently degrading the extracellular matrix, it facilitates reliable subcutaneous delivery of high-dose protein therapeutics. Despite its proven utility, challenges remain in preserving enzyme stability and ensuring consistent catalytic performance across formulations. Recent efforts have therefore focused on excipient and pH optimization to maintain protein integrity while sustaining enzymatic activity, device engineering to enhance injectability and patient usability, and pharmacokinetic modeling to correlate local tissue dispersion with systemic exposure. In oncology, hyaluronidase is increasingly incorporated into anticancer regimens to remodel the tumor microenvironment, alleviate stromal resistance, and promote immune-cell infiltration, thereby enabling synergistic antitumor effects across multiple therapeutic modalities. This review first classifies hyaluronidases by their biological sources and catalytic mechanisms, then summarizes advances in drug delivery with particular emphasis on recombinant human hyaluronidase in clinical use. Finally, it highlights mechanistic and translational insights that guide the rational design of safer, more effective, and clinically adaptable hyaluronidase-enabled delivery systems for both subcutaneous and tumor-targeted applications.

Indexed as

Enzyme-enabled formulationExtracellular matrix remodelingHyaluronidaseSubcutaneous deliveryTranslational pharmacologyTumor targeting

Identifiers

PMID41960159
PMCPMC13059328

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.