Why has nanoparticle engineering become an important strategy for tackling solubility, stability and other drug delivery challenges?
Wu: For poorly soluble drug candidates, various enabling techniques have been used to enhance the apparent solubility and
dissolution rate. Bioavailability can benefit from a higher API concentration achieved by the formation of a supersaturated
solution. However, some compounds exhibit very fast crystallisation and it is extremely difficult to inhibit this property
from a compound’s meta-stable solid-state form (e.g., amorphous or solid dispersions) during shelf-life periods. Moreover,
these compounds will quickly precipitate and/or crystallise in the body, which can significantly reduce the in vivo drug concentration
leading to poor drug efficacy.
Nanoparticle engineering is an alternative method for such compounds in a formulation that uses the special physical property
of nanoparticles. The high-surface area to volume ratio of nanoparticles provides a tremendous driving force for diffusion
so that nanoparticles of a poorly soluble compound can be distributed as nano-sized particles in the body, thereby avoiding
crystallisation or precipitate issues. The smaller size helps to improve the surface–volume ratio of drug candidates, increasing
the dissolution rate and improving API bioavailability.
What advantages does nanoparticle engineering offer over other approaches being used to address solubility and drug delivery
Wu: Several commercialised nanoparticle drug products have successfully demonstrated that nanoparticle engineering can increase
bioavailability and improve pharmacokinetic profile, reducing the frequency of dosing. Furthermore, food–drug interactions
(the food effect) can be reduced because the pharmacokinetic profile of nanoparticle formulations are not affected by the
Fed and Fasted state, as exampled by the cholesterol lowering drug, TriCor (Abbott Laboratories). By using nanoparticle technology,
Janssen’s Invega Sustenna (Xeplion in Europe) became the first once-monthly atypical antipsychotic medicine approved for schizophrenia
in the US. All of these advantages were achieved using nanocrystal technology. Various nanocarrier techniques have also been
used to provide extra benefits in controlled release and targeting delivery.
What popular nanoparticle approaches are currently being exploited by researchers and pharmaceutical companies as part of
efforts to improve drug solubility?
Wu: Two different nanoparticle approaches, nanocrystals and nanocarriers, are being well used by researchers and pharmaceutical
companies. The nanocrystals technique involves decreasing the particle size of a crystalline drug to improve the bioavailability.
Nanocrystals are one of the most successful nanoparticle approaches used so far, evidenced by several commercial drug products,
including Pfizer’s Rapamune, Merck and Co’s Emend, Abbott Laboratories’s TriCor, and Janssen’s Invega Sustenna. They are also
a popular method for proof-of-concept studies, with laboratory-milling equipment and ultrasonic assisted methods being introduced
into laboratories specifically for nanoparticle preparations.
Nanocarriers can be used to deliver drugs more effectively to targeted cells. The use of liposomes is well established in
drug-delivery applications and polymer-based nanocarriers have progressed enormously in recent years, with several applications
demonstrating advantages in targeting delivery, such as Regulon’s Lipop (Liposomal Cisplatin), Cerulean’s CRLX288 (biodegradable
polymeric nanoparticle conjugated to docetaxel and BIND’s Accurin technique for BIND-014 docetaxel.
How are advances in nanoparticle engineering and crystal engineering being combined to tackle the challenges of poor solubility?
What new techniques are emerging that show promise in this area?
Wu: There are two emerging techniques showing promise in the field of nanocrystal techniques. Nanococrystals combines nanoparticle
engineering and crystal engineering for the formulation of nanoparticles. Conventional nanocrystals technology usually focuses
on improving the dissolution rate to enhance bioavailability. Amorphous nanoparticle engineering has also been studied to
increase API concentration. However, the use of nanoparticles of the amorphous drug in the formulation needs to overcome the
challenge in stabilising the amorphous form during both manufacture and the shelf life of the drug product. Nanococrystal
application can potentially increase API concentration without creating disadvantages in the stability and powder properties
of the amorphous form. Another emerging application to the nanocystals technique is the layer-by-layer coating technique applied
to nanoparticles. Coated nanoparticles will not only improve particle stability, but also offer the possibility of designing
nanopaticle surfaces that can achieve controlled release and targeted delivery.