Small molecule-drug conjugates: A novel strategy for cancer-targeted treatment

C Zhuang, X Guan, H Ma, H Cong, W Zhang… - European journal of …, 2019 - Elsevier
Targeted therapy has become an effective strategy of precision medicine for improving
cancer treatment. Selectivity improvement is always popular in modern oncology because of …

Nanomedicine tumor targeting

T Lammers - Advanced Materials, 2024 - Wiley Online Library
Nanomedicines are extensively explored for cancer therapy. By delivering drug molecules
more efficiently to pathological sites and by attenuating their accumulation in healthy organs …

[HTML][HTML] Radiation dosimetry and first therapy results with a 124I/131I-labeled small molecule (MIP-1095) targeting PSMA for prostate cancer therapy

CM Zechmann, A Afshar-Oromieh, T Armor… - European journal of …, 2014 - Springer
Introduction Since the prostate-specific membrane antigen (PSMA) is frequently over-
expressed in prostate cancer (PCa) several PSMA-targeting molecules are under …

[HTML][HTML] Using domain knowledge for robust and generalizable deep learning-based CT-free PET attenuation and scatter correction

R Guo, S Xue, J Hu, H Sari, C Mingels… - Nature …, 2022 - nature.com
Despite the potential of deep learning (DL)-based methods in substituting CT-based PET
attenuation and scatter correction for CT-free PET imaging, a critical bottleneck is their …

Synthesis of [18F]Arenes via the Copper-Mediated [18F]Fluorination of Boronic Acids

AV Mossine, AF Brooks, KJ Makaravage, JM Miller… - Organic …, 2015 - ACS Publications
A copper-mediated radiofluorination of aryl-and vinylboronic acids with K18F is described.
This method exhibits high functional group tolerance and is effective for the radiofluorination …

Antibody–drug conjugates and small molecule–drug conjugates: opportunities and challenges for the development of selective anticancer cytotoxic agents …

G Casi, D Neri - Journal of medicinal chemistry, 2015 - ACS Publications
Conventional cancer chemotherapy heavily relies on the use of cytotoxic agents, which
typically do not preferentially localize at the tumor site and cause toxicity to normal organs …

Chemically defined antibody–and small molecule–drug conjugates for in vivo tumor targeting applications: a comparative analysis

S Cazzamalli, A Dal Corso, F Widmayer… - Journal of the American …, 2018 - ACS Publications
We present the first direct comparative evaluation of an antibody–drug conjugate and of a
small molecule–drug conjugate for cancer therapy, using chemically defined products which …

Radiosyntheses using fluorine-18: the art and science of late stage fluorination

EL Cole, MN Stewart, R Littich… - Current topics in …, 2014 - ingentaconnect.com
Positron (β+) emission tomography (PET) is a powerful, noninvasive tool for the in vivo, three-
dimensional imaging of physiological structures and biochemical pathways. The continued …

PET‐CT Imaging of Polymeric Nanoparticle Tumor Accumulation in Patients

IHC Miedema, GJC Zwezerijnen… - Advanced …, 2022 - Wiley Online Library
Several FDA/EMA‐approved nanomedicines have demonstrated improved
pharmacokinetics and toxicity profiles compared to their conventional chemotherapeutic …

Non‐internalizing antibody–drug conjugates display potent anti‐cancer activity upon proteolytic release of monomethyl auristatin E in the subendothelial extracellular …

R Gébleux, M Stringhini, R Casanova… - … journal of cancer, 2017 - Wiley Online Library
Antibody–drug conjugates (ADCs) represent a promising class of biopharmaceuticals with
the potential to localize at the tumor site and improve the therapeutic index of cytotoxic …