Author
Listed:
- Wenda Wang
(Drexel University, 3141 Chestnut Street, Philadelphia, Pennsylvania 19104, USA)
- Hao Qi
(Drexel University, 3141 Chestnut Street, Philadelphia, Pennsylvania 19104, USA)
- Tian Zhou
(Drexel University, 3141 Chestnut Street, Philadelphia, Pennsylvania 19104, USA)
- Shan Mei
(Drexel University, 3141 Chestnut Street, Philadelphia, Pennsylvania 19104, USA)
- Lin Han
(School of Biomedical Engineering, Science and Health Systems, Drexel University)
- Takeshi Higuchi
(Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 2-1-1, Katahira, Aoba-ku, Sendai 980-8577, Japan)
- Hiroshi Jinnai
(Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 2-1-1, Katahira, Aoba-ku, Sendai 980-8577, Japan)
- Christopher Y. Li
(Drexel University, 3141 Chestnut Street, Philadelphia, Pennsylvania 19104, USA)
Abstract
Lipids and amphiphilic block copolymers spontaneously self-assemble in water to form a plethora of micelles and vesicles. They are typically fluidic in nature and often mechanically weak for applications such as drug delivery and gene therapeutics. Mechanical properties of polymeric materials could be improved by forming crystalline structures. However, most of the self-assembled micelles and vesicles have curved surfaces and precisely tuning crystallization within a nanoscale curved space is challenging, as the curved geometry is incommensurate with crystals having three-dimensional translational symmetry. Herein, we report using a miniemulsion crystallization method to grow nanosized, polymer single-crystal-like capsules. We coin the name crystalsome to describe this unique structure, because they are formed by polymer lamellar crystals and their structure mimics liposomes and polymersomes. Using poly(L-lactic acid) (PLLA) as the model polymer, we show that curved water/p-xylene interface formed by the miniemulsion process can guide the growth of PLLA single crystals. Crystalsomes with the size ranging from ∼148 nm to over 1 μm have been formed. Atomic force microscopy measurement demonstrate a two to three orders of magnitude increase in bending modulus compared with conventional polymersomes. We envisage that this novel structure could shed light on investigating spherical crystallography and drug delivery.
Suggested Citation
Wenda Wang & Hao Qi & Tian Zhou & Shan Mei & Lin Han & Takeshi Higuchi & Hiroshi Jinnai & Christopher Y. Li, 2016.
"Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface,"
Nature Communications, Nature, vol. 7(1), pages 1-6, April.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10599
DOI: 10.1038/ncomms10599
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10599. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.