Fourier Transform Infrared Spectroscopy: Applications to Chemical Systems Vol 1 Edited by J R Ferraro and L J Basile Pp 311 (Academic: New York, San Francisco and London, 1978) $25; £1625

Fourier transform infrared spectroscopy

Approaches for Enhancing Oral Bioavailability of Peptides and Proteins

Mucoadhesive polymers in the design of nano-drug delivery systems for administration by non-parenteral routes: A review

Chitosan is one of the most used polysaccharides in the design of drug delivery strategies for administration of either biomacromolecules or low molecular weight drugs. For these purposes, it is frequently used as matrix forming material in both nano and micron-sized particles. In addition to its interesting physicochemical and biopharmaceutical properties, which include high mucoadhesion and a great capacity to produce drug delivery systems, ensuring the biocompatibility of the drug delivery vehicles is a highly relevant issue. Nevertheless, this subject is not addressed as frequently as desired and even though the application of chitosan carriers has been widely explored, the demonstration of systems biocompatibility is still in its infancy. In this review, addressing the biocompatibility of chitosan carriers with application in drug delivery is discussed and the methods used in vitro and in vivo, exploring the effect of different variables, are described. We further provide a discussion on the pros and cons of used methodologies, as well as on the difficulties arising from the absence of standardization of procedures.

https://www.mdpi.com/2079-4983/3/3/615/pdf?y=1

Biocompatibility of Chitosan Carriers with Application in Drug Delivery

Diatom silica microparticles for sustained release and permeation enhancement following oral delivery of prednisone and mesalamine.

The delivery of therapeutic proteins like insulin, exploiting routes of administration different from the traditional injectable forms, has been investigated extensively, taking advantage of the nanotechnology tools available nowadays in the massive drug delivery system pipeline. In this chapter, we describe in detail the preparation of solid lipid nanoparticles (SLN), further coated with the mucoadhesive polymer chitosan, intended for intestinal absorption of insulin after oral administration. We give special focus on the characterization of the SLN and of the biomacromolecule by itself after encapsulation, because of the intrinsic labile properties of insulin during the manufacturing process. We also describe methods to determine the in vitro intestinal permeability of insulin that solid lipid and chitosan-coated SLN can afford, as well as in vivo models to evaluate the hypoglycemic effect in diabetic animals.

Cláudia Andrade

Papers

Chitosan-coated solid lipid nanoparticles for insulin delivery.