Clinical Trials Directory

Trials / Unknown

UnknownNCT04138342

Topical Fluorescent Nanoparticles Conjugated Somatostatin Analog for Suppression and Bioimaging Breast Cancer

Fluorescent Nanoparticles Conjugated Long-acting Somatostatin Analog for Potent Suppression and Bioimaging Breast Cancer

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Al-Azhar University · Academic / Other
Sex
Female
Age
25 Years – 60 Years
Healthy volunteers
Accepted

Summary

Breast cancer is a communal malignant disease between Saudi females, with a popularity of 21.8%. Since binding to somatostatin receptors (SSTR) induces no immunogenicity in vivo, somatostatin analog (veldoreotide) (VELD) may be suitable for delivering anti-cancer drugs to target and bioimaging the cancer cells. This work aimed to deliver CdS/ZnS core-shell type quantum dots with carboxylic acid-functionalized (QDs-COOH) which is bioimaging and anticancer nanoparticles decorated VELD as SSTR agonist with anti-cancer activity in the form of topical cream to be deposited deep in the breast periphery.

Detailed description

QDs-COOH will be conjugated to the N terminal of phenylalanine of VELD when the reaction proceeded at pH 7. Topical cream will be adapted to deliver the conjugated system for maximum deposition through breast cancer cells using emulsion technology. The formulated nanoparticles and cream will be characterized for size using dynamic light scattering, drug-polymer interaction using FTIR, and morphology using SEM. Cellular uptake, permeability and cell viability study of the successful system of interest will be studied in cell culture models using different breast cell lines. Moreover, the in vivo study will also proceed on rats induced breast cancer. Finally, the nanoparticles loaded in a topical cream will be applied with clinical trial approvement on the human breast cancer for bioimaging and treating breast cancer. This work is to present a novel formulation for treatment and bioimaging of breast cancer which can deliver safely to the patients in a high dose to the affected tumor cells.

Conditions

Interventions

TypeNameDescription
DRUGQuantum dots coated with veldoreotideThe active group will receive Quantum dots coated with veldoreotide in different topical dosage forms as an anti-cancer drug.
DRUGTopical approved placeboThe placebo group will receive topical FDA approved in different dosage forms as a negative control drug.

Timeline

Start date
2019-09-15
Primary completion
2021-06-14
Completion
2022-12-13
First posted
2019-10-24
Last updated
2019-10-24

Locations

4 sites across 2 countries: Egypt, Saudi Arabia

Source: ClinicalTrials.gov record NCT04138342. Inclusion in this directory is not an endorsement.