Evidence map›Paper›PMID 42569871›Full record

ArticleACS applied bio materials2026

Near-Infrared Fluorescence Imaging and Photothermal Therapy of Tumors Using a Targeted Helical Protein Scaffold.

Nicole Carrillo-Malani, Gabrielle Ho, Qiushi Liang, Joann Miller, Theresa M Busch, Ahmad Amirshaghaghi, Zhiliang Cheng, Andrew Tsourkas

Abstract read
In one paragraph

Article in ACS applied bio materials, 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

8 authors.

Nicole Carrillo-MalaniDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.
Gabrielle HoDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.
Qiushi LiangDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.
Joann MillerDepartment of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.
Theresa M BuschDepartment of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.
Ahmad AmirshaghaghiDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.
Zhiliang ChengDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.ORCID 0000-0003-3351-6874
Andrew TsourkasDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.ORCID 0000-0001-7758-1753

Funding

Treating knee osteoarthritis by sPLA2 inhibitor-loaded micellar nanoparticlesR01AR080820 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Zhiliang Cheng · 2022 to 2026
$2.3M
Combined magnetophoresis and photodynamic therapy for the treatment of TNBCR01EB028858 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI TSOURKAS, ANDREW · 2021 to 2024
$1.8M
Image-guided surgery and sonodynamic therapy with stroma-targeted theranostic nanoclustersR01EB029238 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI TSOURKAS, ANDREW · 2020 to 2023
$1.4M
NIAMS NIH HHS R01 AR080820NIBIB NIH HHS R01 EB028858NIBIB NIH HHS R01 EB029238
6 · The paper itself

Abstract

Photothermal therapy (PTT) using near-infrared (NIR) photoactive agents offers a minimally invasive approach for tumor ablation; however, many existing platforms rely on polymeric or nanoparticle carriers that limit targeting precision and control over dye loading. Here, we report the design of a modular eight-helix protein scaffold containing 20 cysteine residues that enables covalent, site-specific conjugation of the NIR dye AQuora800-maleimide. The protein scaffold is expressed with different HER2-targeting ligands, and in vitro screening identifies an affibody dimer-based construct (AD-20AQ) as the most effective platform for targeted fluorescent imaging and therapy. In vivo pharmacokinetic imaging studies in a 4T1 murine tumor model reveal enhanced tumor accumulation of AD-20AQ compared to a monolabeled affibody dimer (AD-1AQ), with sustained retention in HER2-positive tumors. Furthermore, PTT of HER2 tumors with an 808 nm laser, following intravenous administration of AD-20AQ, leads to complete tumor ablation. Collectively, these results establish targeted, labeled protein scaffolds as a versatile platform for NIR fluorescence imaging and photothermal therapy.

Indexed as

Antineoplastic AgentsBiocompatible MaterialsFluorescent DyesOptical ImagingPhotothermal TherapyAnimalsFemaleHumansInfrared RaysMaterials TestingMiceMice, Inbred BALB CParticle SizeAntineoplastic AgentsBiocompatible MaterialsFluorescent Dyesfluorescence imagingmolecular imagingnear-infrared imagingphotothermal therapyprotein scaffold

Identifiers

PMID42569871
PMCPMC13454980

What OpenQuestion holds

Textmetadata
LicenceTDM
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.