Nanopharmaceutical Advanced Delivery Systems. Группа авторов

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СКАЧАТЬ Lipid Carriers

      Temperature-sensitive liposomes were first formulated by Yatvin et al. in 1978 [39], which released a hydrophilic drug at a temperature a few degrees above physiological temperature. The drug release from heat-triggered nanocarriers can be achieved by using thermosensitive polymers. When mild hyperthermia (HT) is applied along with administration of thermosensitive liposomes, the heat increases pore size of tumor vessel, increasing extravasation of liposome into the tumor. Further, hyperthermia facilitates release of drug from thermosensitive liposomes in the tumor vasculature as well as in the tumor interstitium [40].

      The release of drugs occurs at the melting phase transition temperature (T_m) of lipid bilayer following a phase transition from solid gel phase (L_β) to a liquid-crystalline phase (L_α) at T_m. Dipalmitoylphosphatidylcholine, with T_m of 41.4°C, is generally used as a major component in TSL. Drug release characteristics can be modified by blending DPPC with small amounts of other phospholipids, such as 1,2-dioctadecanoyl-sn-glycero-3-phosphocholine (DSPC) (Tm = 54.9°C) [41]. Lysolipid-containing low-temperature-sensitive liposomes (LTSLs) were the first TSL formulations used for intravascular delivery of drugs upon heating. Thermodox^®, licensed to Celsion Corporation (Columbia, MD, USA), is an LTSL formulation loaded with doxorubicin, which is currently under clinical investigation [42]. The shortcomings of LTSL have been rectified by development of sterically stabilized TSL formulation (Stealth TSL) by adding DSPE-PEG2000, which has improved stability and better in vivo half-life as compared to LTSL formulation [43]. Further, the safety of patients using TSL can be assured by encapsulating contrast agents to distinguish heated and unheated tissues, and also, absolute temperatures complementing traditional MRI thermometry methods can be quantified [44, 45].

2.2.2 Micellar Systems

      History of micelles can be traced back to early 1990s [46]. Micelles consist of a hydrophobic core and a hydrophilic shell. The core contains the poorly water-soluble drugs, and the shell protects the core against the aqueous surroundings and protects the micelles from recognition in vivo by the reticuloendothelial system. The micelles can be formulated using either surfactants or polymers [47, 48]. Polymeric micelles exhibit higher stability and solubilization capacity and can be formulated at a lower critical micellar concentration (CMC) when compared to surfactant-based micelles [49]. Moreover, surface of polymers can be engineered through addition of ligands or pH-sensitive moieties for active targeting [47]. For targeting of deep seated tumor, polymeric micelles are a suitable carrier of choice as they can be administered by parenteral route and are biodegradable and exhibit small particle size, high loading capacity, prolonged circulation time, and higher accumulation at tumor site. Kabanov et al. reported enhancement of neuroleptic property of haloperidol when it was formulated in surfactant-based micellar system [50]. Improved cellular uptake and pharmacokinetics of methotrexate was observed when administered in PLGA-soy lecithin micelles [51]. Raza et al. formulated phospholipid-based mixed micelles of tamoxifen for the topical application and reported significantly better controlled release of tamoxifen from mixed micelles over conventional gel system [52].

      2.2.3 Theranostics

      Theranostics are a novel multifunctional approach that can perform both imaging and therapeutic functions. Theranostics nanomedicine provides high loading efficiency and has applications in diagnostics, drug delivery, and therapeutic drug monitoring, especially in the field of personalized medical care [53]. Iron oxide nanoparticles, quantum dots, gold nanoparticles, etc. are the nanoplatforms that are widely used for nanoparticle-based theranostics.

       2.2.3.1 Gold Nanoparticles (AuNPs)

      Gold nanoparticles (AuNPs) provide unique nanoplatform for a variety of applications as in computed tomography (CT), photoacoustics, plasmonic photothermal and photodynamic therapies, and magnetic resonance imaging (MRI) [54]. The AuNPs are available as nanospheres, nanorods, nanocages, nanoshells, and nanostars on large scale. These nanoparticles can be even prepared via green synthesis methods on large scale using extracts of neem leaves [55], Hibiscus rosa sinensis [56], Ocimum tenuiflorum, Azadirachta indica, Mentha spicata leaves, Citrus sinensis [57], Maduca longifolia [58], and Abelmoschus esculentus peel [59]. The antioxidants present in the extracts act as reducing agent for the metal salts, leading to the growth and stabilization of the NPs [60]. The optical characteristics of AuNPs are dependent on their shape and size. AuNPs can enhance scattering of light up to five to six times in comparison to most strongly absorbing organic dyes [61]. AuNPs of larger size undergo scattering and absorption in a similar fashion, and hence, this property of AuNPs can be used for bioimaging [62]. Composition of the nanoparticles also affects their optical properties. Wavelength of surface plasmon resonance (SPR) [63], which determines the specific frequency at which amplitude of oscillation reaches its maxima, changes on incorporation of silica [64].

       2.2.3.2 Iron Oxide Nanoparticles

      Iron oxide nanoparticles are nanoplatforms prepared from magnetite (Fe₃O₄), maghemite (γ-Fe₂O₃), and mixed ferrites (MFe₂O₄ where M = Co, Mn, Ni, or Zn). Iron oxide nanoparticles with particle size less than 200 nm are superparamagnetic, i.e., the particles become magnetized only when there is an external magnetic field. SPIONs are versatile moieties having potential applications in the field of diagnostics and drug delivery. Superparamagnetic iron oxide nanoparticles (SPIONs) are a material of choice as contrast probes for magnetic resonance imaging, and for these applications, coating is done with poly(ethylene glycol) (PEG), poly(vinyl alcohol) (PVA), or natural polysaccharides (dextran and modified chitosan) to provide long shelf lives to these systems. For targeting specific tissues, SPIONS are coupled with antibodies or aptamers and can even be surface-coated with gold and gadolinium ions to enhance the contrasting potential [65]. Nanoparticles with hydrodynamic diameter in the range of 50–150 nm accumulate fast in the mononuclear phagocyte system and can thus be used for liver imaging purposes. For imaging purposes, Ferumoxsil (Lumirem (USA), GastroMARK (EU)) is the only FDA-approved iron oxide nanoparticle. SPIONs coupled with anti-mesothelin antibodies have been studied for targeting pancreatic carcinoma cells and showed no cytotoxicity and high specificity as MRI contrast agents. Similarly, increase in the antitumor immune response was observed with SPIONs coated with membrane Heat Shock Protein 70 (mHSP70) expressed highly on the glioma cells’ surface [66]. Primovist^®, gadolinium-based contrast agents, show specific uptake by hepatocytes instead of macrophages and are specifically used for hepatocellular carcinoma (HCC) detection. Other contrast agents like Ferumoxtran (Combidex^® (USA), Sinerem^® (EU)) and ferumoxytol (Feraheme^® (USA), Rienso^® (EU)) are in clinical trials for lymph node imaging to examine metastatic colonization [67]. By using iron oxide nanoparticles in magnetic particle imaging (MPI), the background noise is reduced drastically, and thus imaging of vascular and cardiac perfusion, as well as cardiac procedures, can be successfully monitored by MPI.

      The SPIONs can also be used in magnetic hyperthermia by application of AMF (alternating magnetic field), which results in change of iron’s magnetization against some resistance forces, thereby releasing heat to the environment. Hyperthermia can be used for stand-alone cancer therapy or as an adjuvant in chemotherapy or radiotherapy [68]. The use of SPIONs as drug carriers is also being studied after modifying hydrophilicity of these nanoparticles with suitable polymers like PEG, PEI (poly(ethylenimine)) [69], PLGA [70], etc. Further, their use as drug carriers can be enhanced by addition of functional groups in order to modify drug release or target binding properties [69].

       2.2.3.3 Quantum Dots

Quantum dots are nanoplatforms made from semiconductor materials as they possess tunable “quantum size effects.” Approximately, 1000 to 100000 СКАЧАТЬ