68Ga-PDT02: PET/CT Radiotracer Performance Data

68Ga-PDT02 is a peptide-based radiotracer targeting the urokinase-type plasminogen activator receptor (uPAR). The dataset likely contains preclinical results including binding affinity (KD = 531.3 nM), in vitro cell uptake, and in vivo PET imaging data from mouse xenograft models. The data was authored by Gangzhong Zhou and uploaded to figshare on 2026-05-07.

Use Cases

• Validate radiotracer binding affinity based on the reported KD value of 531.3 nM
• Compare tumor uptake in preclinical models based on the reported 2.88%ID/mL mean uptake
• Assess pharmacokinetic clearance profiles based on the described rapid renal excretion and low blood retention

Strengths

• Includes specific quantitative metrics: KD = 531.3 nM and mean tumor uptake of 2.88%ID/mL
• Describes a clear experimental workflow from synthesis to in vivo validation
• License is CC-BY-NC-4.0, permitting non-commercial reuse

Limitations

• Dataset size is 4.0 KB, indicating a very limited scope of data
• Column-level documentation is absent; field semantics must be inferred after download
• Row count is unknown, which may limit suitability assessment

Provenance

Source

figshare

Collection Method

Data likely originates from laboratory experiments involving peptide synthesis, radiolabeling, and preclinical imaging.

Freshness

Last updated 2026-05-07 00:44:50