Erlotinib Hydrochloride CAS 183319-69-9: Enhanced Bioavailability and Anticancer Efficacy

Discover the potential of amorphous solid dispersions for improved cancer treatment efficacy with Erlotinib Hydrochloride.

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Advantages of Erlotinib Hydrochloride ASDs

Enhanced Solubility & Dissolution

Amorphous solid dispersions of Erlotinib Hydrochloride demonstrate a marked increase in solubility and dissolution rates, crucial for improving oral absorption and therapeutic outcomes.

Improved Antitumor Activity

Studies show that formulations like ERL + PEG significantly reduce tumor volumes and exhibit superior antitumor efficacy compared to the pure drug, as evidenced by erlotinib hydrochloride anticancer efficacy research.

Reduced Recrystallization Tendency

The use of polymers in ASDs helps stabilize the amorphous state of Erlotinib Hydrochloride, preventing recrystallization and maintaining drug efficacy over time.

Key Applications

Non-Small Cell Lung Cancer (NSCLC) Treatment

Erlotinib Hydrochloride is a targeted therapy used for treating NSCLC, particularly in patients with specific EGFR mutations.

Pancreatic Cancer Therapy

The drug is also employed in combination therapy for advanced pancreatic cancer, demonstrating its versatility in oncology.

Drug Delivery Research

The development of erlotinib hydrochloride amorphous solid dispersion formulations contributes to advancements in drug delivery systems for poorly soluble drugs.

Oncology Drug Development

Research into formulations that improve erlotinib hydrochloride bioavailability enhancement supports the ongoing development of more effective cancer treatments.