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1.
Phys Rev Lett ; 121(4): 046101, 2018 Jul 27.
Article in English | MEDLINE | ID: mdl-30095926

ABSTRACT

Asymmetric light transport has significantly contributed to fundamental science and revolutionized advanced technology in various aspects such as unidirectional photonic devices, optical diodes, and isolators. While metasurfaces mold wave fronts at will with an ultrathin flat optical element, asymmetric transport of light cannot be fundamentally achieved by any linear system including linear metasurfaces. We report asymmetric transport of free-space light at nonlinear metasurfaces upon transmission and reflection. Moreover, we theoretically derive the nonlinear generalized Snell's laws that were experimentally confirmed by the anomalous nonlinear refraction and reflection. The asymmetric transport at optically thin nonlinear interfaces is revealed by the concept of a reversed propagation path. Such an asymmetric transport at metasurfaces opens a new paradigm for free-space ultrathin lightweight optical devices with one-way operation including unrivaled optical valves and diodes.

2.
Adv Mater ; 27(40): 6131-6, 2015 Oct 28.
Article in English | MEDLINE | ID: mdl-26332896

ABSTRACT

Photoelectrochemical etching of silicon can be used to form lateral refractive index gradients for transformation optical devices. This technique allows the fabrication of macroscale devices with large refractive index gradients. Patterned porous layers can also be lifted from the substrate and transferred to other materials, creating more possibilities for novel devices.

3.
Am J Clin Pathol ; 129(2): 309-15, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18208812

ABSTRACT

Routine laboratories use a hemoglobin H (HbH) screen to detect alpha-thalassemia carriers of fatal hemoglobin Bart's hydrops fetalis. This test is laborious and has sensitivity concerns. A commercial zeta-globin enzyme-linked immunosorbent assay (ELISA) is effective in detecting Southeast Asian (SEA) alpha-thalassemia. We present results of a study of the effectiveness of carrier detection of ELISA and a shortened HbH screen compared with gap polymerase chain reaction. ELISA was superior to the HbH screen for the SEA alpha0-thalassemia trait. The ELISA and H screen were equal for detection of all carriers encountered and combined were more effective than either test alone. A positive zeta-globin ELISA result is diagnostic of SEA alpha-thalassemia, and routine use of the zeta-globin ELISA in combination with a shortened HbH screen will improve the efficacy of prenatal screening for carriers of hemoglobin Bart's hydrops fetalis through improved detection and referral for follow-up DNA testing.


Subject(s)
Enzyme-Linked Immunosorbent Assay/methods , Globins/analysis , Hemoglobin H/analysis , alpha-Thalassemia/diagnosis , Adolescent , Adult , Erythrocyte Inclusions/chemistry , Genetic Carrier Screening , Genetic Testing , Humans , Polymerase Chain Reaction
4.
Am J Clin Pathol ; 127(2): 192-6, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17210523

ABSTRACT

In Ontario, Canada, beta-thalassemia is easily detected through measurement of hemoglobin A2, but most laboratories do not do exhaustive DNA investigations for alpha-thalassemia. Therefore, the prevalence of thalassemia in microcytic samples for hemoglobinopathy investigation in Ontario is unknown. To address this, we performed a prospective cohort study in which samples referred for hemoglobinopathy investigation were also evaluated for alpha-thalassemia by DNA testing. Of 800 samples submitted, 664 were evaluable. Of the 664 patients represented, 163 (24.5%) were beta-thalassemia major carriers, 68 (10.2%) were hemoglobin Bart's hydrops fetalis carriers and, in total, 361 (54.4%) had some form of thalassemia. We conclude that microcytosis due to thalassemia is common in Ontario and that major forms of thalassemia, including forms predisposing to hemoglobin Bart's hydrops fetalis and beta-thalassemia major, are frequent. This illustrates the importance of adequate prenatal and laboratory investigation for these abnormalities in Ontario and other similar multiethnic jurisdictions worldwide.


Subject(s)
Anemia, Iron-Deficiency/blood , Hemoglobinometry , Hemoglobinopathies/diagnosis , alpha-Thalassemia/epidemiology , beta-Thalassemia/epidemiology , Adolescent , Anemia, Iron-Deficiency/ethnology , Anemia, Iron-Deficiency/etiology , Anemia, Iron-Deficiency/genetics , Cohort Studies , Erythrocytes, Abnormal/cytology , Hemoglobinopathies/complications , Hemoglobinopathies/ethnology , Humans , Ontario/epidemiology , Prevalence , Prospective Studies , alpha-Thalassemia/complications , alpha-Thalassemia/genetics , beta-Thalassemia/complications , beta-Thalassemia/genetics
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