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Therapeutic Efficacy of Quercetin Versus Its Encapsulated Nanoparticle on Tongue Squamous Cell Carcinoma Cell Line

Cairo University (CU) logo

Cairo University (CU)

Status and phase

Not yet enrolling
Phase 2

Conditions

Oral Cancer

Treatments

Drug: Quercetin-encapsulated PLGA-PEG nanoparticles (Nano-QUT)
Drug: Quercetin 3,3',4',5,6-Pentahydroxyflavone, 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one
Drug: Doxorubicin chemotherapeutic drug as a positive control

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Squamous cell carcinoma (SCC) is the most common oral cavity carcinoma. Conventional therapeutic modalities for oral malignancy include surgery, radiotherapy and chemotherapy alone or in combinations.The major obstacle of using current anticancer drugs is; first the non-specific tissue distribution, as these drugs are unable to distinguish between normal and cancer cells.Quercetin is a bioactive flavonoid having strong antioxidant properties. .Among all the nanomaterials, polymeric nanoparticles are of significant interest for drug delivery applications due to many unique features of nanoparticle polymers.This is the first study to investigate the anticancer effects of (Quercetin) either free or encapsulated by PLGA-PEG NPs in tongue squamous cell carcinoma (TSCC) cell line.

Full description

Squamous cell carcinoma (SCC) is the most common oral cavity carcinoma. Conventional therapeutic modalities for oral malignancy include surgery, radiotherapy and chemotherapy alone or in combinations. The major obstacle of using current anticancer drugs is; first the non-specific tissue distribution, as these drugs are unable to distinguish between normal and cancer cells. Quercetin is a bioactive flavonoid having strong antioxidant properties. It is naturally present in a wide variety of fruits and vegetables. Among all the nanomaterials, polymeric nanoparticles are of significant interest for drug delivery applications due to many unique features of nanoparticle polymers. Polymeric nanocarriers have been fabricated from natural and synthetic polymers. Poly ethylene glycol-poly lactide-co-glycolic acid (PEG-PLGA) amphiphilic copolymer is an emergent system because it can be easily synthesized and possesses a lot of good qualities. Several previous in vitro and in vivo studies have evaluated the cytotoxic effects of quercetin and have revealed that it decreases cell viability and increases cell apoptotic rate in OSCC. However, the anti-cancer property of quercetin in tongue squamous cell carcinoma (TSCC) has not been studied yet. This is the first study to investigate the anticancer effects of (Quercetin) either free or encapsulated by PLGA-PEG NPs in tongue squamous cell carcinoma (TSCC) cell line.

Enrollment

1,000,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Tongue Squamous cell carcinoma cell lines
  • Quercetin drug.
  • Quercetin-encapsulated PLGA-PEG nanoparticles (Nano-QUT)
  • Application of a Quercetin drug as chemotherapeutic drug.
  • Detection of Quercetin activity in apoptosis or cytotoxicity/cell viability.

Exclusion criteria

  • Any cancer cell line other than tongue Squamous cell carcinoma cell lines
  • Any use of Quercetin other than chemotherapy.
  • Detection of Quercetin activities other than apoptosis or cytotoxicity/cell viability

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

1,000,000 participants in 3 patient groups

Quercetin drug.
Experimental group
Treatment:
Drug: Quercetin 3,3',4',5,6-Pentahydroxyflavone, 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one
Quercetin-encapsulated PLGA-PEG nanoparticles
Experimental group
Treatment:
Drug: Quercetin-encapsulated PLGA-PEG nanoparticles (Nano-QUT)
Doxorubicin chemotherapeutic drug
Active Comparator group
Treatment:
Drug: Doxorubicin chemotherapeutic drug as a positive control

Trial contacts and locations

1

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Central trial contact

Hana'a Algadi, P.h.D

Data sourced from clinicaltrials.gov

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