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Vanton Research Laboratory is a contract research company dedicated to developing next generation drug delivery systems and products for pharmaceutical applications.

Vanton also conducts stability programs for clients (R&D batches, registration batches, and commercial batches), and has in-house research programs, developing new pipeline products for out-licensing.

Current Research and Pipeline Products
  • Developing for clients various matrix diffusion tablet/capsule systems for oral sustained/controlled release (usually patentable)
  • Designing and developing for client oral disintegration sustained release tablets (ODT-SR) – usually patentable
  • Molecular Caging (MC) processed delivery systems for sustained release formulations. MC technology is applicable to solid, liquid, gel, for oral or parenteral administrations.
  • Micro and nano particles/capsules and non-conventional delivery systems – usually patentable
  • Other types of delivery system (emulsions, micelles, liposome formulations, etc.)
Techniques
  • Matrix diffusion tablet/capsule systems for oral sustained/controlled release
  • Oral disintegration sustained release tablets
  • Molecular Caging (MC) processed dosage forms for various sustained release formulations applicable to solid, liquid, gel, and for oral or parenteral administrations. Micro and nano particles/capsules and non-conventional delivery systems.
  • Liposome formulations
Technology Platforms

Vanton Patented Drug Delivery Technologies

  • Molecular caging platform ( a know-how process Vanton develops for each client’s specific API and dosage form. It is a highly API depending system, applicable to both oral and parenteral administrations
  • Orally disintegrating tablet with sustained release (ODT-SR) capability for improving patient compliance and for special applications
  • A know-how process for constructing transdermal and topical formulations that can be controlled to deliver drugs for (1) topical, (2) epi-dermis, (3), dermis, and/or systemic c applications

Emulsions

  • Semi-solid and liquid emulsion delivery systems for parenteral sustained release dosage forms
  • Liquid or solid powder formulations for re-constitution (injection or infusion)

Micro and Nano Particle/Capsules

  • Micro and nano delivery systems for oral and parenteral sustained release dosage forms

The Drug Development Timeline and Vanton Services

From Drug Discovery to Product Launch, Vanton can help you develop custom, patentable products.

From: Drug Discovery

Drug Substance

Pre-formulation
– Soluability
– Drug Sensitivity
Drug Stability

Product Development

Novel Formulations
Novel Delivery Systems
Product Development
Patent Strategy

Analysis

Methods Development /Validation
GMP Analyses – Datasheet System
Stability Testing
Non-Conventional Analysis

GLP

GLP Manufacturing
Pre-IND Documents

Clinical Manufacturing (Phase I, II, III)

GMP Manufacturing
– Tablets/Capsules
– Transdermal Patches
– Liquids /Creams
IND CMC Documents

Stability Program

Clinical Stability Program
– Assay/Content Uniformity
– Dissolution
– Purity
– Hardness/Water content
– Microbial Testing
To: NDA / Product Launch

Vanton Labs can help you move your product development forward.

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