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      Nanosponges- Versatile Platform as Drug Carrier

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          Abstract

          Background:

          Recently nano-drug delivery systems has become integral part of the most novel drug delivery systems and has gained considerable importance owing to various advantages such as carrier for poorly soluble drugs; targeting of the molecules at desired site; protection from degradation etc.

          Methods:

          In current review we conducted systemic search of literature and patent inventions focusing on nanosponges. The summary of search was inclusive of various aspects of nanosponges such as drugs characteristics to be considered while incorporating in nanosponges, other crucial additive during formulation of nanosponges, methods of preparation, characterization and applications of nanosponges in pharmaceuticals.

          Results:

          Nanosponges are nanocarriers for both lipophilic and hydrophilic drugs. These are prepared by different methods such as emulsion-solvent evaporation, solvent method, melting method, ultrasound assisted method etc. and all these methods were less time consuming, more economic and evaluated by sophisticated techniques available for routine analysis. These are among the most feasible alternative to address several formulation difficulties associated with the physicochemical properties of the drug. Porous nature and small particle size are vital properties of the nanosponges that contribute crucially to correct the drawbacks of the drug. The properties of the nanosponges can be enhanced when these were combined with cyclodextrins. Numerous research work was carried out to explore the cyclodextrin based nanosponges. Besides, it is also used for smart targeting to tumors and for drug release in a sustainable pattern. Nanosponges can be prepared by simple method These can be tuned to release the drug by different routes so as to achieve the maximum benefits of the drug.

          Conclusion:

          Numerous research work carried out on the nanosponges as drug carrier. The method of preparation and characterization of nanosponges are quite economic and routinely available. Owing to potential benefits and probable applications these can be used as efficient carrier for certain drugs. The authors expect that the current review will act as guide to investigate the nanosponges as nanodrug delivery system.

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          Most cited references88

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          Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization.

          Cyclodextrins are cyclic oligosaccharides which have recently been recognized as useful pharmaceutical excipients. The molecular structure of these glucose derivatives, which approximates a truncated cone or torus, generates a hydrophilic exterior surface and a nonpolar cavity interior. As such, cyclodextrins can interact with appropriately sized molecules to result in the formation of inclusion complexes. These noncovalent complexes offer a variety of physicochemical advantages over the unmanipulated drugs including the possibility for increased water solubility and solution stability. Further, chemical modification to the parent cyclodextrin can result in an increase in the extent of drug complexation and interaction. In this short review, the effects of substitution on various cyclodextrin properties and the forces involved in the drug-cyclodextrin complex formation are discussed. Some general observations are made predicting drug solubilization by cyclodextrins. In addition, methods which are useful in the optimization of complexation efficacy are reviewed. Finally, the stabilizing/destabilizing effects of cyclodextrins on chemically labile drugs are evaluated.
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            Cyclodextrin-based nanosponges for delivery of resveratrol: in vitro characterisation, stability, cytotoxicity and permeation study.

            The aim of this work was to increase the solubility, stability and permeation of resveratrol by complexation with cyclodextrin-based nanosponges (NS). Nanosponges are recently developed hyper-cross-linked cyclodextrin polymers nanostructured to form three-dimensional networks; they are obtained by reacting cyclodextrin with a cross-linker such as carbonyldiimidazole. They have been used to increase the solubility and stability of poorly soluble actives. This study aimed at formulating complexes of resveratrol with β-cyclodextrin nanosponges in different weight ratios. DSC, FTIR and X-ray powder diffraction (XRPD) studies confirmed the interaction of resveratrol with NS. XRPD showed that the crystallinity of resveratrol decrease after encapsulation. The particle sizes of resveratrol-loaded NS are in between 400 to 500 nm with low polydispersity indices. Zeta potential is sufficiently high to obtain a stable colloidal nanosuspension. TEM measurement also revealed a particle size around 400 nm for NS complexes. The in vitro release and stability of resveratrol complex were increased compared with plain drug. Cytotoxic studies on HCPC-I cell showed that resveratrol formulations were more cytotoxic than plain resveratrol. The permeation study indicates that the resveratrol NS formulation showed good permeation in pigskin. The accumulation study in rabbit mucosa showed better accumulation of resveratrol NS formulation than plain drug. These results signify that resveratrol NS formulation can be used for buccal delivery and topical application.
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              Green synthesis of silver and palladium nanoparticles at room temperature using coffee and tea extract

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Recent Patents on Nanotechnology
                NANOTEC
                Bentham Science Publishers Ltd.
                18722105
                June 2023
                June 2023
                : 17
                : 2
                : 91-103
                Affiliations
                [1 ]Department of Pharmaceutics, JSPMS Rajarshi Shahu College of Pharmacy and Research, Tathwade, Pune, Maharashtra, 411033, India
                [2 ]Department of Pharmacology, School of Pharmacy, Dr. Vishwanath Karad MIT World Peace University, Kothrud, Pune, Maharashtra, 411038, India
                [3 ]Technical lead, HCL Technologies, Chennai, Tamil Nadu 600119, India
                [4 ]Department of Pharmacognosy, JSPMs Charak College of Pharmacy Wagholi, Pune, Maharashtra, 412207, India
                [5 ]Department of Pharmaceutical Chemistry, Shardabai Pawar Institute of Pharmaceutical Sciences and Research, Sharadanagar, Nira Road, Baramati, Maharashtra, 413115, India
                Article
                10.2174/1872210516666220905092202
                36748244
                6385bb44-8482-4629-8622-319ae90e875b
                © 2023
                History

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