Abstract

Aerogels are the lightest processed solid materials on Earth and with the largest empty volume fraction in their structure. Composition versatility, modularity, and feasibility of industrial scale manufacturing are behind the fast emergence of aerogels in the drug delivery field. Compared to other 3D materials, the high porosity (interconnected mesopores) and high specific surface area of aerogels may allow faster loading of small-molecule drugs, less constrained access to inner regions of the matrix, and more efficient interactions of the biological milieu with the polymer matrix. Processing in supercritical CO2 medium for both aerogel production (drying) and drug loading (impregnation) has remarkable advantages such as absence of an oxidizing environment, clean manufacture, and easiness for the scale-up under good manufacturing practices. The aerogel solid skeleton dictates the chemical affinity to the different drugs, which in turn determines the loading efficiency and the release pattern. Aerogels can be used to increase the solubility of BCS Class II and IV drugs because the drug can be deposited in amorphous state onto the large surface area of the skeleton, which facilitates a rapid contact with the body fluids, dissolution, and release. Conversely, tuning the aerogel structure by functionalization with drug-binding moieties or stimuli-responsive components, application of coatings and incorporation of drug-loaded aerogels into other matrices may enable site-specific, stimuli-responsive, or prolonged drug release. The present review deals with last decade advances in aerogels for drug delivery. An special focus is paid first on the loading efficiency of active ingredients and release kinetics under biorelevant conditions. Subsequent sections deal with aerogels intended to address specific therapeutic demands. In addition to oral delivery, the physical properties of the aerogels appear to be very advantageous for mucosal administration routes, such as pulmonary, nasal, or transdermal. A specific section devoted to recent achievements in gene therapy and theranostics is also included. In the last section, scale up strategies and life cycle assessment are comprehensively addressed.

Highlights

  • Processing of advanced materials as aerogels has opened new ways of addressing a variety of technological challenges while fulfilling ecofriendly criteria

  • A similar coating technology with Eudragit® L 30 D-55 applied to alginate-starch aerogels demonstrated the usefulness of the coating to preserve the aerogel structure during storage in environments of high relative hu­ midity [129]. These results showed the feasibility of adapting a coating technology well-established in the pharmaceutical industry to the processing of drug-loaded aerogels

  • The drug-loaded silica aerogel particles that released more than 80% of the cargo in the first hour in contact with phosphate buffer saline (PBS), whereas the multi-layer composite sustained the release for more than 6 h following a nonFickian mechanism (n =0.62–0.66) with the PVA swelling contrib­ uting to the control of drug release [135]

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Summary

Introduction

Processing of advanced materials as aerogels has opened new ways of addressing a variety of technological challenges while fulfilling ecofriendly criteria. Production of aerogels applying supercritical processing involves several changes of the liquid phase with organic solvents and subsequent extraction/drying under supercritical conditions (commonly in the presence of supercritical CO2; scCO2) This processing avoids the liquid-gas surface tension and liquid-solid adhesive forces and, there­ fore, prevents the collapse of the original pores [16]. (GMP) are remarkable advantages from the perspective of manufacturing of pharmaceutical grade products [18,19] Another limitation is that once the drug-loaded aerogel is adminis­ tered to the body, the large surface contact area with the physiological media may lead to fast and uncontrolled drug release, especially if the solubility and partition coefficient of the drug into the body fluids are high [11]. Engineering-based scale up strategies and life cycle assessment are addressed in the last section of this review

Drug loading modalities and outcomes
Drug release mechanisms
Aerogels for oral administration
Aerogels as drug solubilizing aids
Aerogels for sustained and stimuli-responsive release
Coated and core-shell aerogels
Aerogels for topical and transdermal administration
Aerogels for pulmonary and nasal administration
Scale-up and life cycle assessment
Findings
Conclusions and future perspectives
Full Text
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