Porous inorganic nanostructured materials are widely used nowadays as drug delivery carriers due to their adventurous features: suitable architecture, large surface area and stability in the biological fluids. Among the different types of inorganic porous materials, silica, calcium carbonate, and calcium phosphate have received significant attention in the last decade. The use of porous inorganic materials as drug carriers for cancer therapy, gene delivery etc. has the potential to improve the life expectancy of the patients affected by the disease. The main goal of this review is to provide general information on the current state of the art of synthesis of the inorganic porous particles based on silica, calcium carbonate and calcium phosphate. Special focus is dedicated to the loading capacity, controllable release of drugs under internal biological stimuli (e.g., pH, redox, enzymes) and external noninvasive stimuli (e.g., light, magnetic field, and ultrasound). Moreover, the diverse compounds to deliver with silica, calcium carbonate and calcium phosphate particles, ranging from the commercial drugs to genetic materials are also discussed.

Carefully designed micro-and nanocarriers can provide significant advantages over conventional macroscopic counterparts in biomedical applications. The set of requirements including a high loading capacity, triggered release mechanisms, biocompatibility, and biodegradability should be considered for the successful delivery realization. Porous calcium carbonate (CaCO3) is one of the most promising platforms, which can encompass all the beforehand mentioned requirements. Here, we study both the particles formation and biological applicability of CaCO3. In particular, anisotropic differently shaped CaCO3 particles were synthesized using green sustainable approach based on co-precipitation of calcium chloride and sodium carbonate/bicarbonate at different ratios in the presence of organic additives. The impact of salts concentrations, reaction time, as well as organic additives was systematically researched to achieve controllable and reliable design of CaCO3 particles. It has been demonstrated that the crystallinity (vaterite or calcite phase) of particles depends on the initial salts' concentrations. The loading capacity of prepared CaCO3 particles is determined by their surface properties such as specific surface area, pore size and zetapotential. Differently shaped CaCO3 particles (spheroids, ellipsoids, toroids) were used to evaluate their uptake efficiency on the example of C6 glioma cells. The results show that the ellipsoidal particles possess a higher probability for internalization by cancer cells. All tested particles were also found to have a good biocompatibility. The capability to design physicochemical properties of CaCO3 particles has a significant impact on drug delivery applications, since the particles geometry substantially affects cell behavior (internalization, toxicity) and allows outperforming standard spherical counterparts.

Cell functionalization with recently developed various nano- and microcarriers for therapeutics has significantly expanded the application of cell therapy and targeted drug delivery for the effective treatment of a number of diseases. The aim of this progress report is to review the most recent advances in cell-based drug vehicles designed as biological transporter platforms for the targeted delivery of different drugs. For the design of cell-based drug vehicles, different pathways of cell functionalization, such as covalent and noncovalent surface modifications, internalization of carriers are considered in greater detail together with approaches for cell visualization in vivo. In addition, several animal models for the study of cell-assisted drug delivery are discussed. Finally, possible future developments and applications of cell-assisted drug vehicles toward targeted transport of drugs to a designated location with no or minimal immune response and toxicity are addressed in light of new pathways in the field of nanomedicine.