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Handbook of Vitamin C Research

Handbook of Vitamin C Research

Handbook of Vitamin C Research

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Encapsulation Devices for <strong>Vitamin</strong> C 201<strong>Vitamin</strong> C/Eudragit® microspheres obtained by spray-drying method were unable toslow down the release <strong>of</strong> the drug with respect to the free form <strong>of</strong> ascorbic acid but thesemicrospheres showed a good morphology and size distribution that permit to propose them ascandidate for the delivery <strong>of</strong> vitamin C as associated therapy in the treatment <strong>of</strong> colorectalcancer by oral route [71].The procedure <strong>of</strong> obtaining microparticles with encapsulated ascorbic acid by spraydrying was described by Finotelli and co-workers [112]. The morphology <strong>of</strong> theCapsul/vitamin C particles was observed by a scanning electron microscopy, whose analysisshowed a tendency <strong>of</strong> agglomeration. Particle size analysis showed a multi-modal particlesize distribution, but with a main mode in intermediate diameters range (4–8 μm). Theparticle yield was 52%. Ascorbic acid stability was studied for particles stored, at both, roomtemperature and at 45°C showing 100% <strong>of</strong> retention at the beginning. Microcapsulescontaining 20% <strong>of</strong> ascorbic acid recovered by a mixture presented 7% <strong>of</strong> ascorbic acidreduction in samples for up to 60 days stored at 28°C temperature.Spray drying technique was also used by Desai and co-workers for encapsulation <strong>of</strong>vitamin C in tripolyphosphate cross-linked chitosan microspheres [59, 116-118]. Resultsshowed a mean particle size <strong>of</strong> 6.1-9.0 µm which was influenced by the amount <strong>of</strong> crosslinkingagent. Encapsulation efficiency was around 58% but decreased as the amount <strong>of</strong>tripolyphosphate solution increased. The amount <strong>of</strong> crosslinking affected the release rate andparticle size.8. Applications <strong>of</strong> Micro and Nanoparticleswith Ascorbic AcidIn recent years, micro and nanoparticles have attracted considerable attention as potentialdrug delivery devices in view <strong>of</strong> their applications in the controlled release <strong>of</strong> drugs, theirability to target particular organs/tissues, as carriers <strong>of</strong> DNA in gene therapy, and in theirability to deliver divers drugs through a different route <strong>of</strong> administration [91].Encapsulation <strong>of</strong> vitamin C within micro or nanoparticles proposes many advantages.Primarily, encapsulation can help to stabilise vitamin C. Many studies have been done on thisvitamin with variables optimized to determine the most stable way <strong>of</strong> encapsulating vitaminC and to give the highest retention possible [87]. Particles containing encapsulated ascorbicacid can be used in numerous applications. Numerous products are using currently vitamin Cbecause <strong>of</strong> its significant properties, particularly its anti-oxidizing effect. <strong>Vitamin</strong> C hasability <strong>of</strong> quenching or stabilizing free radicals that lead over time to degenerative diseases,including cancer, cardiovascular disease, cataracts, and other diseases.PLGA nanospheres are very efficient mean <strong>of</strong> transdermal transport <strong>of</strong> medicaments inthe body, e.g. ascorbic acid [133, 134].Ascorbic acid providing photoprotective capabilities by inhibiting UVA and UVBradiation-induced damage by neutralizing the oxygen-free radicals in the skin, it prevents UVimmunosuppression, stimulates collagen synthesis and has anti-inflammatory properties [135,136]. Here, not only does encapsulation provide a convenient formulation vehicle, but it alsoenhanced the stability <strong>of</strong> the encapsulated payload at an elevated temperature.

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