Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Sep;12(3):157-162.
doi: 10.14797/mdcj-12-3-157.

Novel Nanoprinting for Oral Delivery of Poorly Soluble Drugs

Affiliations
Review

Novel Nanoprinting for Oral Delivery of Poorly Soluble Drugs

Cihan Yilmaz et al. Methodist Debakey Cardiovasc J. 2016 Sep.

Abstract

Many of the newly developed drugs for cancer, and some of those for cardiovascular disease, are poorly soluble in water and cannot be taken orally. This can be overcome by employing a new and effective delivery system utilizing nanotechnology. We present a new method for oral preparation of poorly soluble drugs that entails assembling (printing) drug-loaded polymeric micelles into sub-100 nm orally acceptable nanorods (NRs). Due to their small size, these NRs will have a high permeability through cells and thus should transport through the intestine to allow for drug delivery in the blood. These NRs drugs are expected to penetrate tumors more efficiently and much faster than individual nanoparticles and may also be useful for drug delivery to atherosclerotic plaque. This should lead to better bioavailability of the drug with reduced toxicity and side effects. Currently used micellar formulations are administered intravenously, which is invasive and could be toxic due to high doses and interaction with normal healthy tissues. Oral drug administration is the easiest and most desirable way to deliver most drugs, including those that are poorly soluble.

Keywords: drug-loaded micelles; nanoparticles; nanorods; poorly soluble drugs.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Fabrication of 3D nanorods (NRs) fabricated by fast and scalable directed assembly method. (a) Schematic of fabrication process. (b) Billions of NRs fabricated on a substrate. (c) 30-nm diameter NR fabricated from PEG-PE micelles. (d) 100-nm diameter NR fabricated from paclitaxel drug-loaded PEG-PE. PEG-PE: polyethylene glycol-phosphatidylethanolamine
Figure 2.
Figure 2.
(a) Preparation of a paclitaxel drug-loaded tagged micellar system. (b) Fabrication and harvesting of orally acceptable 3-dimensional drug-loaded micellar nanorods (NRs) using electric field directed assembly. Red and black colors of the NRs indicate the dye and the drug incorporated into micelles, respectively. (c) Optical and scanning electron microscopy images of the drug-loaded micelles embedded in a water-soluble polymer before and after harvested from the substrate.
Figure 3.
Figure 3.
Product concept from the production of the drug-loaded nanorods to delivery to the tumor cells.

Similar articles

Cited by

References

    1. Savjani KT, Gajjar AK, Savjani JK.. Drug solubility: importance and enhancement techniques. ISRN Pharm. 2012; 2012: 195727. - PMC - PubMed
    1. Matsumura Y, Maeda H. A new concept for macromolecular therapeutics in cancer chemotherapy: mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs. Cancer Res. 1986. December; 46( 12 Pt 1): 6387– 92. - PubMed
    1. Maeda H, Wu J, Sawa T, Matsumura Y, Hori K.. Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. J Control Release. 2000. March 1; 65( 1–2): 271– 84. - PubMed
    1. Maeda H, Sawa T, Konno T.. Mechanism of tumor-targeted delivery of macromolecular drugs, including the EPR effect in solid tumor and clinical overview of the prototype polymeric drug SMANCS. J Control Release. 2001. July 6; 74( 1–3): 47– 61. - PubMed
    1. Maeda H. The enhanced permeability and retention (EPR) effect in tumor vasculature: the key role of tumor-selective macromolecular drug targeting. Adv Enzyme Regul. 2001; 41: 189– 207. - PubMed

LinkOut - more resources