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Nanotechnology in Medicine. Группа авторовЧитать онлайн книгу.

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(PEI), poly(ε‐caprolactone) (PCL), poly‐N‐(2‐hydroxypropyl) methacrylamide (HPMA), poly(D,L‐lactic acid) (PLA), dextran, poly(D,L‐lactic‐co‐glycolic acid) (PLGA), alongside additional stealth effect offered by most widely used PEG (Utreja et al. 2020). The amphiphilic character allows poorly water‐soluble drugs to be loaded in the core with the shell providing aqueous solubility, colloidal stability, and essential stealth character. Although these nanoformulations offer improved penetrability, solubility, bioavailability, targeting through directing ligand complexed on the surface or combining monoclonal antibodies to the micelle corona, they suffer from poor in vivo stability. This effect is due to dissociation and early drug release below critical micelle concentration succeeding its administration that can also lead to drug‐related toxicity. However, stimuli‐responsive cross‐linked micelles have exhibited micellar stability and have attracted formulation scientists for the delivery of docetaxel, camptothecin, paclitaxel, cisplatin, and oxaliplatin (Ventola 2017).

      The original milled organic nanocrystal, Rapamune®, approved by FDA in 2000 opened new avenues for resourceful NPs that were capable of enhancing solubility and bioavailability. Nanocrystal‐based drugs within the range of 1000 nm are peculiar because they are solely composed of drug derivatives without any carriers bound to them and are typically stabilized using polymeric steric stabilizers or surfactants. The poorly soluble organic or inorganic drugs are rendered enriched pharmacokinetic (PK)/pharmacodynamic (PD) properties by nanostructures known as nanocrystals. Nanocrystals have unique characteristics that allow them to solve problems such as increasing solubility of saturation, increased speed of dissolution, and enhanced surface/cell membrane binding. Saturation solubility increases the forces that, via biological mechanisms, such as the walls of the gastrointestinal tract, drive diffusion‐based mass transfer (Farjadian et al. 2019). The oral absorption process for nanocrystal formulations, however, is not well known and their action is not completely predictable after subcutaneous injection. They are photochemically stable and exhibit a narrow, controllable, symmetric emission spectrum. They consist of an optically energetic core enclosed by a shield that creates a physical barrier to the external environment, rendering them less vulnerable to photo‐oxidation or medium shifts. The methods of preparation of nanocrystals can be divided into top‐down and bottom‐up processes. The bottom‐up method creates nanocrystals from the solution, which requires two basic stages: nucleation and crystal formation. It mainly involves high‐pressure homogenization accompanied by grinding procedures. The top‐down methodologies comprise of high‐energy mechanical powers like milling (NanoCrystals®) or high‐pressure homogenization (IDD‐P®, DissoCubes® and Nanopure®), and the main benefit is that it is adaptable to the manufacturing scale (Lopalco and Denora 2018). Nevertheless, high energy, cost, and time used as well as impurity from grinding media are a downside of this technology, leading to unintended toxic undesirable results. Supercritical fluid (SCF) such as supercritical carbon dioxide exhibits superior physical characteristics, liquid solubilization, diffusivity similar to gas and minimal environmental effect. Thus, nanocrystals are lately prepared using SCF.

      1.3.3 Tissue Engineering and Regenerative Medicine

Schematic illustration of nanomaterial applications in tissue engineering and regenerative medicine.
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